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

Urinometer, Electrical

21 CFR 876.1800 / Gastroenterology, Urology
FDA source (opens on fda.gov)

EXS is the FDA product code for Urinometer, Electrical, a class II device type, regulated under 21 CFR 876.1800. As of , FDA records hold no 510(k) clearances under this code and 6 recalls.

Classification record

Product code
EXS
Device name
Urinometer, Electrical
Regulation
21 CFR 876.1800
Device class
Class II
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
0
Ingested recalls
6

Companies listing this code with FDA

Companies whose registered establishments list this code