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

Cannula, Suction, Uterine

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

HGH is the FDA product code for Cannula, Suction, Uterine, a class II device type, regulated under 21 CFR 884.5070. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HGH
Device name
Cannula, Suction, Uterine
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
6
Ingested recalls
0

Clearances, product code HGH

By decision year
6 clearances under product code HGH with a decision year between 1984 and 2018, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HGH by decision year
YearClearances
19841
19941
20101
20151
20171
20181

Applicants with the most clearances

Product code HGH
Applicants holding the most 510(k) clearances under product code HGH
ApplicantClearances
Chongquin Jinshan Science & Technology (Group) Co., Ltd.1
Dongguan Microview Medical Technology Co., Ltd.1
Imex Medical Systems, Inc.1
Kolster Methods1
Panpac Medical Corporation1
Womancare Global1

Companies listing this code with FDA

Companies whose registered establishments list this code