HHFClass I

Remover, Intrauterine Device, Contraceptive, Hook-Type

21 CFR 884.4530 / Obstetrics/Gynecology

HHF is the FDA product code for Remover, Intrauterine Device, Contraceptive, Hook-Type, a class I device type, regulated under 21 CFR 884.4530. As of 2026-09-10, FDA records hold 6 510(k) clearances under this code, the most recent dated 1994-02-24, and one recall.

Classification record

Product code: HHF
Device name: Remover, Intrauterine Device, Contraceptive, Hook-Type
Regulation: 21 CFR 884.4530
Device class: Class I
Review panel: Obstetrics/Gynecology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 6
Ingested recalls: 1

Clearances, product code HHF

By decision year

6 clearances under product code HHF with a decision year between 1981 and 1994, 1981 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code HHF by decision year
Year	Clearances
1981	1
1982	1
1983	1
1984	1
1989	1
1994	1

Applicants with the most clearances

Product code HHF

Applicants holding the most 510(k) clearances under product code HHF
Applicant	Clearances
Proto-Med, Inc.	2
F. & F. Koenigkramer	1
Premier Dental Products Co	1
Thomasville Medical Assoc.	1
Zinnanti Surgical Instruments, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 52 companies shown, in name order