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

Bottle, Hot/Cold Water

21 CFR 880.6085 / General Hospital
FDA source (opens on fda.gov)

FPF is the FDA product code for Bottle, Hot/Cold Water, a class I device type, regulated under 21 CFR 880.6085. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FPF
Device name
Bottle, Hot/Cold Water
Regulation
21 CFR 880.6085
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code FPF

By decision year
1 clearance under product code FPF with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FPF by decision year
YearClearances
19791

Applicants with the most clearances

Product code FPF
Applicants holding the most 510(k) clearances under product code FPF
ApplicantClearances
3M Company1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 73 companies shown, in name order