BTP — Dropper, Ether Class I

FDA Device Classification

FDA product code BTP covers "Dropper, Ether", a Class I medical device regulated under 21 CFR 868.5420. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
BTP
Device Class
Class I
Regulation Number
868.5420
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K093126hospitech respirationANAPNOGUARD ENDOTRACHEAL TUBEMarch 2, 2010