SUTURE REMOVAL PAK— 510(k) K801746

Name: FDA 510(k) clearance K801746
Creator: U.S. Food and Drug Administration
Published: 1980-08-20

Substantially Equivalent

Devco Medical Industries, Inc.

FDA 510(k) clearance K801746 for SUTURE REMOVAL PAK, Substantially Equivalent on 1980-08-20. Applicant: Devco Medical Industries, Inc.. Device class: 1.

Clearance details

Applicant: Devco Medical Industries, Inc.
Product code: Code FZT
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1980-07-28
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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