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
BRTClass I

Restraint, Patient, Conductive

21 CFR 880.6760 / General Hospital
FDA source (opens on fda.gov)

BRT is the FDA product code for Restraint, Patient, Conductive, a class I device type, regulated under 21 CFR 880.6760. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
BRT
Device name
Restraint, Patient, Conductive
Regulation
21 CFR 880.6760
Device class
Class I
Review panel
General Hospital
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
0

Companies listing this code with FDA

Companies whose registered establishments list this code