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

Controller, Abortion Unit, Vacuum

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

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

Classification record

Product code
HGG
Device name
Controller, 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
1
Ingested recalls
0

Clearances, product code HGG

By decision year
1 clearance under product code HGG with a decision year between 1988 and 1988, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HGG by decision year
YearClearances
19881

Applicants with the most clearances

Product code HGG
Applicants holding the most 510(k) clearances under product code HGG
ApplicantClearances
Galenica Enterprises, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code HGG.