510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HFFClass II

Aspirator, Endometrial

21 CFR 884.1060 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HFF is the FDA product code for Aspirator, Endometrial, a class II device type, regulated under 21 CFR 884.1060. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HFF
Device name
Aspirator, Endometrial
Regulation
21 CFR 884.1060
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
5
Ingested recalls
0

Clearances, product code HFF

By decision year
5 clearances under product code HFF with a decision year between 1982 and 2004, 1991 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HFF by decision year
YearClearances
19821
19841
19912
20041

Applicants with the most clearances

Product code HFF
Applicants holding the most 510(k) clearances under product code HFF
ApplicantClearances
Axcan Scientific Corp.2
Gynetics Medical Products NV1
Gynopharma, Inc.1
CooperSurgical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code