BWL — Apparatus, Electronanesthesia Class III

FDA Device Classification

FDA product code BWL covers "Apparatus, Electronanesthesia", a Class III medical device regulated under 21 CFR 868.5400. Submissions are reviewed by the Anesthesiology panel.

Classification Details

Product Code
BWL
Device Class
Class III
Regulation Number
868.5400
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Definition

Call for PMAs 12/26/96 (61 FR 50706 (9/27/96))