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

COX DISPOSABLE POLYPECTOMY SNARES

K Number: K923671 · Decision Oct 13, 1992
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
15
Review Days
83

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Basic Information

Device Name
COX DISPOSABLE POLYPECTOMY SNARES
K Number
K923671
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cox Medical Ent., Inc.
Date Received
July 22, 1992
Decision Date
October 13, 1992
Product Code
FDI
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
FDI Snare, Flexible

Similar 510(k) Clearances

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Other Clearances by Cox Medical Ent., Inc.

K Number Device Name
K946360 MODULAR BIOPSY FORCEP
K950689 UCB
K941464 BASICS ENDOSCOPY SYSTEM
K940911 BASICS ENDOSCOPY SYSTEM
K932790 THERMAL OPTION
K935250 ACCU-PATH
K924655 COX DISPOSABLE ENDOSCOPE CLEANING BRUSH(CB-X2)
K923672 COX DISPOSABLE ENDOSCOPE CLEANING BRUSH
K923489 COX DISPOSABLE RETRIEVAL DEVICES
K914466 COX DISPOSABLE CYTOLOGY BRUSHES
Search all 15 clearances from Cox Medical Ent., Inc. →