RESUABLE HOT BIOPSY FORCEPS— 510(k) K972505

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K972505 for RESUABLE HOT BIOPSY FORCEPS, Substantially Equivalent on 1997-09-18. Applicant: United States Endoscopy Group, Inc.. Device class: 2.

Clearance details

Applicant
United States Endoscopy Group, Inc.
Product code
Code KGE
Device class
Class 2
Regulation
21 CFR 876.4300
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mentor, OH, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KGE

view all

More clearances from United States Endoscopy Group, Inc.

view all

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