Medical Device Manufacturer · US , Walker , MI

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

24 submissions · 22 cleared · Since 1984

Total

Cleared

Denied

Aequitron Medical, Inc. has 22 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 22 cleared submissions from 1984 to 1997. Primary specialty: Anesthesiology.

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

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

24 devices

1-12 of 24

Cleared Apr 18, 1997

MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR

K961972 · BZQ

Anesthesiology · 333d

Cleared Jun 20, 1996

MODEL LP-1000 VOLUME VENTILATOR

K952880 · CBK

Anesthesiology · 364d

Cleared Nov 08, 1994

OXYGEN CONCENTRATION INDICATOR

K944654 · CCL

Anesthesiology · 48d

Cleared Sep 10, 1992

MODEL 6213 REMOTE ALARM

K914424 · CBK

Anesthesiology · 343d

Cleared Mar 11, 1992

PORTABLE OXYGEN GENERATOR

K915381 · CAW

Anesthesiology · 103d

Cleared Sep 19, 1991

NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)

K911399 · DZD

Dental · 174d

Cleared Apr 10, 1991

RESPIRATION/HEART RATE MONITOR MODEL 9500/9550

K903020 · BZQ

Anesthesiology · 273d

Cleared Nov 30, 1990

CONTINUOUS VOLUME VENTILATOR MODEL LP10

K903010 · CBK

Anesthesiology · 142d

Cleared Nov 30, 1990

MODEL LP6 VENTILATOR, MODIFICATION

K905244 · CBK

Anesthesiology · 10d

Cleared Jul 13, 1990

MODEL 9200 RESPIRATION/HEART RATE MONITOR

K901656 · BZQ

Anesthesiology · 94d

Cleared Jul 13, 1990

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON

K902785 · BZQ

Anesthesiology · 17d

Cleared May 22, 1990

MODEL 9101 RECORDER/ANALYZER SYSTEM

K901251 · DSH

Cardiovascular · 67d

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

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