FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GUSBERG HYSTERECTOMY CLAMP

K Number: K771344 · Decision Jul 27, 1977
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
1
Applicant Total
18
Review Days
14

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Basic Information

Device Name
GUSBERG HYSTERECTOMY CLAMP
K Number
K771344
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4520
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
J. Sklar Mfg. Co., Inc.
Date Received
July 13, 1977
Decision Date
July 27, 1977
Product Code
HGC
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
HGC Clamp, Uterine

Similar 510(k) Clearances

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Other Clearances by J. Sklar Mfg. Co., Inc.

K Number Device Name
K843693 JACOBS HIGH VACUUM SUCTION UNIT 05-2570
K842112 TISCHLER CERVICAL BIOPSY PUNCH FORCEPS
K842111 KOGAN ENDOSPECULUM 9-1/2
K822448 SCISSORS, VARIOUS
K802457 KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610
K802458 KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611
K801273 MAGILL CATHETER INTRO. FORCEPS
K800441 RUDD-CLINIC HEMORRHOIDAL FORCEPS
K790577 HEMORRHOIDAL LIGATOR
K772230 CANNULA, PERFUSION, FALLOPIAN TUBE
Search all 18 clearances from J. Sklar Mfg. Co., Inc. →