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
FHFClass II

System, Evacuator, Fluid

21 CFR 876.4370 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FHF is the FDA product code for System, Evacuator, Fluid, a class II device type, regulated under 21 CFR 876.4370. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FHF
Device name
System, Evacuator, Fluid
Regulation
21 CFR 876.4370
Device class
Class II
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
3
Ingested recalls
0

Clearances, product code FHF

By decision year
3 clearances under product code FHF with a decision year between 1977 and 2010, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FHF by decision year
YearClearances
19771
20011
20101

Applicants with the most clearances

Product code FHF
Applicants holding the most 510(k) clearances under product code FHF
ApplicantClearances
Applied Medical1
Modern Medical Equipment Mfg., Ltd.1
The Minnesota Back Brace Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code