HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD— 510(k) K992390

Name: FDA 510(k) clearance K992390
Creator: U.S. Food and Drug Administration
Published: 1999-12-22

Substantially Equivalent

Telemed Systems, Inc.

FDA 510(k) clearance K992390 for HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD, Substantially Equivalent on 1999-12-22. Applicant: Telemed Systems, Inc.. Device class: 2.

Clearance details

Applicant: Telemed Systems, Inc.
Product code: Code KGE
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 1999-07-19
Decision date: 1999-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlborough, MA, US

Download summary PDF View on FDA.gov ↗

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