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

GOMCO CIRCUMCISION CLAMP

K Number: K926535 · Decision Feb 25, 1994
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
25
Applicant Total
33
Review Days
422

Basic Information

Device Name
GOMCO CIRCUMCISION CLAMP
K Number
K926535
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
THOMASVILLE MEDICAL ASSOC.
Date Received
December 30, 1992
Decision Date
February 25, 1994
Product Code
HFX
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HFX Clamp, Circumcision

Similar 510(k) Clearances

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

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Other Clearances by THOMASVILLE MEDICAL ASSOC.

K Number Device Name
K926429 VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
K926536 DISPOSABLE PLASTIC VAGINAL SPECULA
K926484 CORSON MYOMA GRASPING FORCEPS
K926527 ROTO FIT BIOPSY FORCEPS
K930030 SUCTION TUBES: HOUSE, BARON
K926531 HYSTERECTOMY FORCEPS
K926533 Z-CLAMP FORCEPS
K926540 SOPHER AND BIERER OVUM FORCEPS
K926471 MOGAN CIRCUMCISION CLAMP
K926532 ENDO CERVICAL CURETTE
Search all 33 clearances from THOMASVILLE MEDICAL ASSOC. →