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

Urinal

21 CFR 880.6730 / General Hospital
FDA source (opens on fda.gov)

FNP is the FDA product code for Urinal, a class I device type, regulated under 21 CFR 880.6730. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FNP
Device name
Urinal
Regulation
21 CFR 880.6730
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 FNP

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

Applicants with the most clearances

Product code FNP
Applicants holding the most 510(k) clearances under product code FNP
ApplicantClearances
Bemis Health Care1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 101 companies shown, in name order