DSR — Stimulator, Carotid Sinus Nerve Class III

FDA Device Classification

FDA product code DSR covers "Stimulator, Carotid Sinus Nerve", a Class III medical device regulated under 21 CFR 870.3850. Submissions are reviewed by the Cardiovascular panel. Devices under this code are implants.

Classification Details

Product Code
DSR
Device Class
Class III
Regulation Number
870.3850
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
Yes

Definition

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