SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES— 510(k) K024011

Name: FDA 510(k) clearance K024011
Creator: U.S. Food and Drug Administration
Published: 2002-12-19

Substantially Equivalent

Surgical Instruments Service and Savings, Inc.

FDA 510(k) clearance K024011 for SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES, Substantially Equivalent on 2002-12-19. Applicant: Surgical Instruments Service and Savings, Inc.. Device class: 2.

Clearance details

Applicant: Surgical Instruments Service and Savings, Inc.
Product code: Code NLU
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 2002-12-04
Decision date: 2002-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sisters, OR, 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
K011800 — VANGUARD REPROCESSED ELECTRIC BIOPSY FORCEPS2001-09-27

More clearances from Surgical Instruments Service and Savings, Inc.

view all

K124033 — MEDISISS REPROCESSED ULTRASONIC INSTRUMENTS2014-01-07
K031869 — SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES2003-12-24
K030179 — MEDISISS PHACOEMULSIFICATION TIPS/NEEDLES2003-01-24
K012644 — REPROCESSED TROCARS AND CANNULAS2002-07-29
K012669 — REPROCESSED ELECTROSURGICAL ELECTRODES2002-06-27

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