REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS— 510(k) K022751

Name: FDA 510(k) clearance K022751
Creator: U.S. Food and Drug Administration
Published: 2002-11-04

Substantially Equivalent

Medical Device Services

FDA 510(k) clearance K022751 for REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS, Substantially Equivalent on 2002-11-04. Applicant: Medical Device Services. Device class: 2.

Clearance details

Applicant: Medical Device Services
Product code: Code KGE
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 2002-08-19
Decision date: 2002-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. George, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KGE

view all

K251807 — Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR2026-03-06
K250187 — Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)2025-10-07
K242857 — ClearHemograsper2025-05-21
K231721 — Disposable Hot Biopsy Forceps2023-12-14
K220053 — Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI2022-02-04

More clearances from Medical Device Services

view all

K022753 — REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS2002-11-14
K022743 — REPROCESSED DISPOSABLE TROCARS2002-10-09
K022748 — REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS2002-10-09
K022744 — REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS2002-09-18

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