Medical Device Manufacturer · US , Walker , MI

Aequitron Medical, Inc. - FDA 510(k) Cleared Devices

24 submissions · 22 cleared · Since 1984

Recent clearances: MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR, MODEL LP-1000 VOLUME VENTILATOR, OXYGEN CONCENTRATION INDICATOR

24

Total

22

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aequitron Medical, Inc. Cardiovascular ✕

5 devices

1-5 of 5

Cleared May 22, 1990

MODEL 9101 RECORDER/ANALYZER SYSTEM

Cardiovascular · 67d

Cleared Oct 30, 1984

IMPEDANCE/8200 MONITOR-MODEL 8300

Cardiovascular · 278d

Cleared Oct 02, 1984

HEART RATE/RESPIRATION SIMULATOR 8310

Cardiovascular · 183d

Cleared Apr 17, 1984

RESPIRATION/8100-HEART RATE RECORDER

Cardiovascular · 203d

Cleared Apr 17, 1984

EVENT TAPE RECORDER 8293

Cardiovascular · 203d