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

Selector, Size, Ostomy

21 CFR 876.5900 / Gastroenterology, Urology
FDA source (opens on fda.gov)

EXA is the FDA product code for Selector, Size, Ostomy, a class I device type, regulated under 21 CFR 876.5900. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EXA
Device name
Selector, Size, Ostomy
Regulation
21 CFR 876.5900
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code EXA

By decision year
1 clearance under product code EXA with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EXA by decision year
YearClearances
19781

Applicants with the most clearances

Product code EXA
Applicants holding the most 510(k) clearances under product code EXA
ApplicantClearances
C.R. Bard Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code