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

Circulator, Breathing-Circuit

21 CFR 868.5250 / Anesthesiology
FDA source (opens on fda.gov)

CAG is the FDA product code for Circulator, Breathing-Circuit, a class II device type, regulated under 21 CFR 868.5250. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
CAG
Device name
Circulator, Breathing-Circuit
Regulation
21 CFR 868.5250
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code