Biopsy Forceps— 510(k) K252722

Substantially Equivalent

Fehling Instruments GmbH

FDA 510(k) clearance K252722 for Biopsy Forceps, Substantially Equivalent on 2025-09-30. Applicant: Fehling Instruments GmbH. Device class: 2.

Clearance details

Applicant: Fehling Instruments GmbH
Product code: Code DWZ
Device class: Class 2
Regulation: 21 CFR 870.4075
Advisory panel: Cardiovascular
Date received: 2025-08-28
Decision date: 2025-09-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Karlstein, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code DWZ

K170726 — Biopsy Forceps2017-06-02
K072051 — NOVATOME, MODEL: SU101-502007-10-03
K010473 — SPARROWHAWK DISPOSABLE2001-06-06
K000409 — MODIFICATION TO T-REX BIOPSY FORCEPS2000-02-28
K991486 — ULTRA-CBX1999-11-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.