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

Ring, Laparotomy

21 CFR 876.4730 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FHI is the FDA product code for Ring, Laparotomy, a class I device type, regulated under 21 CFR 876.4730. As of , FDA records hold no 510(k) clearances under this code and 10 recalls.

Classification record

Product code
FHI
Device name
Ring, Laparotomy
Regulation
21 CFR 876.4730
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
10

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order