HHKClass II

Curette, Suction, Endometrial (And Accessories)

21 CFR 884.1175 / Obstetrics/Gynecology

HHK is the FDA product code for Curette, Suction, Endometrial (And Accessories), a class II device type, regulated under 21 CFR 884.1175. As of 2026-09-10, FDA records hold 42 510(k) clearances under this code, the most recent dated 2025-10-16, and 3 recalls.

Classification record

Product code: HHK
Device name: Curette, Suction, Endometrial (And Accessories)
Regulation: 21 CFR 884.1175
Device class: Class II
Review panel: Obstetrics/Gynecology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 42
Ingested recalls: 3

Clearances, product code HHK

By decision year

42 clearances under product code HHK with a decision year between 1976 and 2025, 2000 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code HHK by decision year
Year	Clearances
1976	1
1977	3
1978	1
1979	2
1980	1
1981	2
1982	3
1986	2
1987	1
1988	2
1992	3
1995	2
1996	1
1998	1
1999	3
2000	4
2002	1
2003	1
2004	1
2005	1
2010	1
2011	1
2020	2
2024	1
2025	1

Applicants with the most clearances

Product code HHK

Applicants holding the most 510(k) clearances under product code HHK
Applicant	Clearances
American Hospital Supply	2
Crossbay Medical	2
Milex Products, Inc.	2
Pioneer Medical, Inc.	2
Ri Mos. S.r.l.	2
Select Medical Systems, Inc.	2
CooperSurgical, Inc.	1
Berkeley Medevices	1
Bioteque America Inc	1
Bioteque Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 41 companies shown, in name order