INTEGUSEAL MICROBIAL SEALANT, MODEL IS 100 AND 1S200— 510(k) K052870

Name: FDA 510(k) clearance K052870
Creator: U.S. Food and Drug Administration
Published: 2006-09-29

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K052870 for INTEGUSEAL MICROBIAL SEALANT, MODEL IS 100 AND 1S200, Substantially Equivalent on 2006-09-29. Applicant: Kimberly-Clark Corp.. Device class: 2.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code NZP
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2005-10-11
Decision date: 2006-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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