Biopsy Forceps— 510(k) K170726

Name: FDA 510(k) clearance K170726
Creator: U.S. Food and Drug Administration
Published: 2017-06-02

Substantially Equivalent

Fehling Instruments GmbH & Co. KG

FDA 510(k) clearance K170726 for Biopsy Forceps, Substantially Equivalent on 2017-06-02. Applicant: Fehling Instruments GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Fehling Instruments GmbH & Co. KG
Product code: Code DWZ
Device class: Class 2
Regulation: 21 CFR 870.4075
Advisory panel: Cardiovascular
Date received: 2017-03-09
Decision date: 2017-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Karlstein, DE

Download summary PDF View on FDA.gov ↗

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K000409 — MODIFICATION TO T-REX BIOPSY FORCEPS2000-02-28
K991486 — ULTRA-CBX1999-11-05

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