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

Source, Abortion Unit, Vacuum

21 CFR 884.5070 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HGF is the FDA product code for Source, Abortion Unit, Vacuum, a class II device type, regulated under 21 CFR 884.5070. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HGF
Device name
Source, Abortion Unit, Vacuum
Regulation
21 CFR 884.5070
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
4
Ingested recalls
0

Clearances, product code HGF

By decision year
4 clearances under product code HGF with a decision year between 1989 and 1995, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HGF by decision year
YearClearances
19891
19901
19911
19951

Applicants with the most clearances

Product code HGF
Applicants holding the most 510(k) clearances under product code HGF
ApplicantClearances
Charles L. Rose and Co., Inc.1
Douglas James Donaldson Compliance Services1
Hgm Medical Laser Systems, Inc.1
Medgyn Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code