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

Tent, Pediatric Aerosol

21 CFR 868.5710 / Anesthesiology
FDA source (opens on fda.gov)

FNC is the FDA product code for Tent, Pediatric Aerosol, a class II device type, regulated under 21 CFR 868.5710. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FNC
Device name
Tent, Pediatric Aerosol
Regulation
21 CFR 868.5710
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code FNC

By decision year
1 clearance under product code FNC with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FNC by decision year
YearClearances
19891

Applicants with the most clearances

Product code FNC
Applicants holding the most 510(k) clearances under product code FNC
ApplicantClearances
Cal-Trends Products1

Companies listing this code with FDA

Companies whose registered establishments list this code

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