SEPP ADHESIVE REMOVER— 510(k) K934790

Name: FDA 510(k) clearance K934790
Creator: U.S. Food and Drug Administration
Published: 1994-03-11

Substantially Equivalent

Medi-Flex Hospital Products, Inc.

FDA 510(k) clearance K934790 for SEPP ADHESIVE REMOVER, Substantially Equivalent on 1994-03-11. Applicant: Medi-Flex Hospital Products, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Flex Hospital Products, Inc.
Product code: Code KOX
Device class: Class 1
Regulation: 21 CFR 878.4730
Advisory panel: General, Plastic Surgery
Date received: 1993-10-05
Decision date: 1994-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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