REPROCESSED MULTIPLE CLIP APPLIERS— 510(k) K033579

Name: FDA 510(k) clearance K033579
Creator: U.S. Food and Drug Administration
Published: 2005-07-11

Substantially Equivalent

Clearmedical, Inc.

FDA 510(k) clearance K033579 for REPROCESSED MULTIPLE CLIP APPLIERS, Substantially Equivalent on 2005-07-11. Applicant: Clearmedical, Inc.. Device class: 2.

Clearance details

Applicant: Clearmedical, Inc.
Product code: Code NMJ
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2003-11-13
Decision date: 2005-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellevue, WA, US

Download summary PDF View on FDA.gov ↗

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K033593 — REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS2003-11-20
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