VANGUARD REPROCESSED ELECTRIC BIOPSY FORCEPS— 510(k) K011800

Name: FDA 510(k) clearance K011800
Creator: U.S. Food and Drug Administration
Published: 2001-09-27

Substantially Equivalent

Vanguard Medical Concepts, Inc.

FDA 510(k) clearance K011800 for VANGUARD REPROCESSED ELECTRIC BIOPSY FORCEPS, Substantially Equivalent on 2001-09-27. Applicant: Vanguard Medical Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Vanguard Medical Concepts, Inc.
Product code: Code NLU
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 2001-06-08
Decision date: 2001-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeland, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NLU

view all

K050136 — REPROCESSED HOT BIOPSY FORCEPS2005-07-20
K033593 — REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS2003-11-20
K024011 — SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES2002-12-19

More clearances from Vanguard Medical Concepts, Inc.

view all

K053051 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES2005-12-22
K051616 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES2005-09-06
K051180 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES2005-07-22
K051043 — VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS2005-06-06
K050763 — VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS2005-06-01

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