510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
BTBClass I

Hook, Ether

21 CFR 868.5420 / Anesthesiology
FDA source (opens on fda.gov)

BTB is the FDA product code for Hook, Ether, a class I device type, regulated under 21 CFR 868.5420. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
BTB
Device name
Hook, Ether
Regulation
21 CFR 868.5420
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code