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
LHFClass II

Warmer, Microwave, Infusion Fluid

21 CFR 880.5725 / General Hospital
FDA source (opens on fda.gov)

LHF is the FDA product code for Warmer, Microwave, Infusion Fluid, a class II device type, regulated under 21 CFR 880.5725. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LHF
Device name
Warmer, Microwave, Infusion Fluid
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
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 LHF

By decision year
2 clearances under product code LHF with a decision year between 1981 and 1981, 1981 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LHF by decision year
YearClearances
19812

Applicants with the most clearances

Product code LHF
Applicants holding the most 510(k) clearances under product code LHF
ApplicantClearances
Downs Surgical, Ltd.1
Travenol Laboratories, S.A.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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