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

Pad, Kelly

21 CFR 878.4370 / General, Plastic Surgery
FDA source (opens on fda.gov)

FNW is the FDA product code for Pad, Kelly, a class II device type, regulated under 21 CFR 878.4370. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FNW
Device name
Pad, Kelly
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FNW

By decision year
2 clearances under product code FNW with a decision year between 1984 and 1984, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FNW by decision year
YearClearances
19842

Applicants with the most clearances

Product code FNW
Applicants holding the most 510(k) clearances under product code FNW
ApplicantClearances
Pmt, Inc.1
Reagent Laboratory, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code