REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS— 510(k) K033593

Substantially Equivalent

Clearmedical, Inc.

FDA 510(k) clearance K033593 for REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS, Substantially Equivalent on 2003-11-20. Applicant: Clearmedical, Inc.. Device class: 2.

Clearance details

Applicant
Clearmedical, Inc.
Product code
Code NLU
Device class
Class 2
Regulation
21 CFR 876.4300
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Bellevue, WA, US
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