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

Aspirator, Endocervical

21 CFR 884.1050 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HFC is the FDA product code for Aspirator, Endocervical, a class II device type, regulated under 21 CFR 884.1050. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HFC
Device name
Aspirator, Endocervical
Regulation
21 CFR 884.1050
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
11
Ingested recalls
0

Clearances, product code HFC

By decision year
11 clearances under product code HFC with a decision year between 1980 and 1997, 1990 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code HFC by decision year
YearClearances
19801
19811
19821
19891
19903
19951
19962
19971

Applicants with the most clearances

Product code HFC
Applicants holding the most 510(k) clearances under product code HFC
ApplicantClearances
Cook Incorporated2
A & A Medical, Inc.1
Customed, Inc1
Fertility Instrumentation, Inc.1
Innovative Medical Products, Inc.1
Permobil, AB1
Robert Hasselbrack, M.D.1
Seamless Hospital Products Co.1
Select Medical Systems, Inc.1
Unimar, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code