Medical Device Manufacturer · US , Clearwater , FL

Sensidyne, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000
4
Total
4
Cleared
0
Denied

Sensidyne, Inc. has 4 FDA 510(k) cleared medical devices. Based in Clearwater, US.

Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Sensidyne, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sensidyne, Inc.
4 devices
1-4 of 4
Cleared May 13, 2002
SENSAID, MODELS# RC-NVA30-10
K021246 · DQA
Anesthesiology · 24d
Cleared Feb 12, 2002
SENSAID
K011974 · DQA
Anesthesiology · 232d
Cleared Mar 01, 2001
100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-I
K010382 · CCL
Anesthesiology · 21d
Cleared Aug 31, 2000
SENSIDYNE OXYGEN ANALYZER & SENSIDYNE OXYGEN MONITOR
K000700 · CCL
Anesthesiology · 183d
Filters
Filter by Specialty
All4 Anesthesiology 4