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

Clamp, Uterine

21 CFR 884.4520 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HGC is the FDA product code for Clamp, Uterine, a class I device type, regulated under 21 CFR 884.4520. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 11 recalls.

Classification record

Product code
HGC
Device name
Clamp, Uterine
Regulation
21 CFR 884.4520
Device class
Class I
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
11

Clearances, product code HGC

By decision year
2 clearances under product code HGC with a decision year between 1977 and 1989, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HGC by decision year
YearClearances
19771
19891

Applicants with the most clearances

Product code HGC
Applicants holding the most 510(k) clearances under product code HGC
ApplicantClearances
J. Sklar Mfg. Co., Inc.1
Zinnanti Surgical Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order