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

IUD HOOKS

K Number: K926541 · Decision Feb 24, 1994
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
5
Applicant Total
33
Review Days
421

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Basic Information

Device Name
IUD HOOKS
K Number
K926541
Device Class
FDA class 1
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 24, 1994
Product Code
HHF
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
HHF Remover, Intrauterine Device, Contraceptive, Hook-Type

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HHF), 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
K926531 HYSTERECTOMY FORCEPS
K926527 ROTO FIT BIOPSY FORCEPS
K926535 GOMCO CIRCUMCISION CLAMP
K926533 Z-CLAMP FORCEPS
K926540 SOPHER AND BIERER OVUM FORCEPS
K926532 ENDO CERVICAL CURETTE
K926536 DISPOSABLE PLASTIC VAGINAL SPECULA
K930030 SUCTION TUBES: HOUSE, BARON
K926484 CORSON MYOMA GRASPING FORCEPS
Search all 33 clearances from Thomasville Medical Assoc. →