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

COMEG ENDOSCOPY GRASPING FORCEPS

K Number: K970489 · Decision Mar 19, 1997
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
51
Applicant Total
3
Review Days
37

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Basic Information

Device Name
COMEG ENDOSCOPY GRASPING FORCEPS
K Number
K970489
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4680
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Comeg Endoscopy
Date Received
February 10, 1997
Decision Date
March 19, 1997
Product Code
FFL
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
FFL Dislodger, Stone, Basket, Ureteral, Metal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FFL), ordered by most recent decision date.

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Other Clearances by Comeg Endoscopy

K Number Device Name
K971881 COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTORS
K970764 COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES