Medical Device Manufacturer · US , Washington , DC

Dickstein, Shapiro & Morin - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dickstein, Shapiro & Morin Anesthesiology ✕

2 devices

1-2 of 2

Cleared Sep 24, 1986

RESPICENTRAL(TM)

Anesthesiology · 13d

Cleared Jun 13, 1986

RESPISOMNOGRAPH

Anesthesiology · 66d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 28, 2026