510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FHTClass II

Set, Gavage, Infant, Sterile

21 CFR 876.5980 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FHT is the FDA product code for Set, Gavage, Infant, Sterile, a class II device type, regulated under 21 CFR 876.5980. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FHT
Device name
Set, Gavage, Infant, Sterile
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
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 FHT

By decision year
1 clearance under product code FHT with a decision year between 1980 and 1980, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FHT by decision year
YearClearances
19801

Applicants with the most clearances

Product code FHT
Applicants holding the most 510(k) clearances under product code FHT
ApplicantClearances
Ethox Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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