Medical Device Manufacturer · US , Plano , TX

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

4 submissions · 4 cleared · Since 2004

Recent clearances: MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER, MEDIAID PULSE OXIMETER M30 AND M34, MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mediaid, Inc. Anesthesiology ✕

4 devices

1-4 of 4

Cleared May 02, 2008

MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER

Anesthesiology · 319d

Cleared Nov 05, 2007

MEDIAID PULSE OXIMETER M30 AND M34

Anesthesiology · 145d

Cleared Apr 12, 2007

MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N

Anesthesiology · 283d

Cleared Sep 14, 2004

MEDIAID REUSABLE FINGER CLIP SPO2 SENSORS AND DISPOSABLE NON-ADHESIVE SENSORS...

Anesthesiology · 55d