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

Bell, Circumcision

21 CFR 884.4530 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

FHG is the FDA product code for Bell, Circumcision, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FHG
Device name
Bell, Circumcision
Regulation
21 CFR 884.4530
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
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FHG

By decision year
2 clearances under product code FHG with a decision year between 1977 and 1991, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FHG by decision year
YearClearances
19771
19911

Applicants with the most clearances

Product code FHG
Applicants holding the most 510(k) clearances under product code FHG
ApplicantClearances
American Hospital Supply1
Edward Weck, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code