DSRClass IIIImplant
Stimulator, Carotid Sinus Nerve
Cardiovascular · 21 CFR 870.3850
Call for PMAs 12/26/96 (61 FR 50706 (9/27/96))
MDR events416All time
Recalls0All time
Registered firms4Currently listed
510(k) clearances0All time
Recent MDR events
416 adverse event reports on file
- Barostim Neo2Jul 30, 2026InjuryCvrx, Inc3007972010-2026-00090
- Barostim Neo2Jul 28, 2026InjuryCvrx, Inc3007972010-2026-00089
- Barostim Neo2Jul 27, 2026InjuryCvrx, Inc3007972010-2026-00087
- Barostim Neo2Jul 27, 2026InjuryCvrx, Inc3007972010-2026-00088
- BAROSTIM NEO2Jul 22, 2026InjuryCvrx, Inc3007972010-2026-00086
- BAROSTIM NEO2Jul 17, 2026InjuryCvrx, Inc3007972010-2026-00085
- BAROSTIM NEO2Jul 17, 2026InjuryCvrx, Inc3007972010-2026-00082
- BAROSTIM NEO2Jul 15, 2026InjuryCvrx, Inc3007972010-2026-00083
- BAROSTIM NEO2Jul 15, 2026InjuryCvrx, Inc.3007972010-2026-00084
- BAROSTIM NEO2Jul 13, 2026InjuryCvrx, Inc3007972010-2026-00081
Event type breakdown
Injury381
Death31
Malfunction4
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
4 firms currently registered for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.
PMA approvals
1 premarket approvals for this product code