LARSONASSOCIATESREALTYBusiness Directories,Company Directories

Company Name: Corporate Name:	LARSONASSOCIATESREALTY
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Company Address:	1216tlnticv,BENSON,MN,USA
ZIP Code: Postal Code:	56215
Telephone Number:	5075329155 (+1-507-532-9155)
Fax Number:	5075324668 (+1-507-532-4668)
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USA SIC Code(Standard Industrial Classification Code):	653118
USA SIC Description:	Real Estate
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eCFR :: 21 CFR 807. 87 -- Information required in a premarket . . .
§ 807 87 Information required in a premarket notification submission Each premarket notification submission shall contain the following information: (a) The device name, including both the trade or proprietary name and the common or usual name or classification name of the device
CFR - Code of Federal Regulations Title 21
For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR) Note: If you need help accessing information in different file formats, see
Premarket Notification Truthful And Accurate Statement | FDA
Premarket Notification Truthful and Accurate Statement as required by 21 CFR 807 87 (k)
21 CFR § 807. 87 Information required in a premarket notification . . .
CFR Title 21 Section 807 87 Information required in a premarket notification submission of the Electronic Code of Federal Regulations
21 CFR 807. 87 - Information required in a premarket notification . . .
21 CFR 807 87 - Information required in a premarket notification submission View the most recent version of this document on this website
21 CFR § 807. 87 - LII Legal Information Institute
§ 807 87 Information required in a premarket notification submission Each premarket notification submission shall contain the following information: (a) The device name, including both the trade or proprietary name and the common or usual name or classification name of the device
21 CFR Part 807 Subpart E -- Premarket Notification Procedures
§ 807 87 Information required in a premarket notification submission Each premarket notification submission shall contain the following information: (a) The device name, including both the trade or proprietary name and the common or usual name or classification name of the device
Guidance for Industry and FDA Staff Dental Handpieces - Premarket . . .
vides all of the information and data required under 21 CFR 807 87 and described in this guidance Traditional 510(k) should include all of your methods, data, acceptance criteria, and
21 CFR Part 807 - Subpart E - Premarket Notification Procedures
§ 807 92 Content and format of a 510 (k) summary § 807 93 Content and format of a 510 (k) statement § 807 94 Format of a class III certification § 807 95 Confidentiality of information § 807 97 Misbranding by reference to premarket notification § 807 100 FDA action on a premarket notification
Food and Drug Administration, HHS §80 - GovInfo
The device was in commercial dis-tribution before May 28, 1976; or A premarket notification submis-sion was filed by another person 807 87 Information required in a pre-market notification submission