FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR

K Number: K974312 · Decision Jan 21, 1998
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
22
Review Days
65

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Basic Information

Device Name
REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR
K Number
K974312
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Telemed Systems, Inc.
Date Received
November 17, 1997
Decision Date
January 21, 1998
Product Code
KNW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNW Instrument, Biopsy

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Other Clearances by Telemed Systems, Inc.

K Number Device Name
K020379 PPD BALLOON DILATATION CATHETER
K013737 MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOON
K010412 FLEXIBLE ENDOSCOPIC SCISSORS
K992390 HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD
K992402 5.0 FRENCH X 200CM X 35MM TIP TAPER-20MM CUTTING WIRE, 5.0 FRENCH X 200CM X 35MM TIP TAPER-30MM CUTTING WIRE, 5.0 FRENCH
K974300 TELEMED SYSTEMS RETRIEVAL BASKET
K901435 GASTROINTESTINAL CYTOLOGY BRUSH
K901427 BILIARY STONE RETRIEVAL AND OCCLUSION BALLOON
K901425 PYLORIC BALLOON DILATOR
K901424 ESOPHAGEAL BALLOON DILATOR
Search all 22 clearances from Telemed Systems, Inc. →