Medical Device Manufacturer · US , Corona Del Mar , CA

Pegasus Research Corp. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1988

Total

Cleared

Denied

Pegasus Research Corp. has 12 FDA 510(k) cleared anesthesiology devices. Based in Corona Del Mar, US.

Historical record: 12 cleared submissions from 1988 to 2012.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pegasus Research Corp.

12 devices

1-12 of 12

Cleared Nov 07, 2012

HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL...

K122857 · CAF

Anesthesiology · 50d

Cleared Apr 26, 2004

PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY

K020700 · BTT

Anesthesiology · 784d

Cleared Feb 21, 2003

PMH 1000 HEATED HUMIDIFIER

K013856 · BTT

Anesthesiology · 472d

Cleared Oct 24, 2000

HEATED HUMIDIFIER

K983783 · BTT

Anesthesiology · 728d

Cleared Feb 28, 1997

THERA-MIST NEBULIZER MODEL-P3000

K962534 · CAF

Anesthesiology · 245d

Cleared May 05, 1995

AQUALARM MOISTURE SENSOR MODEL P85000

K946057 · BYH

Anesthesiology · 144d

Cleared Jun 24, 1992

AUTOCLAVABLE THERA-MIST HUMIDIFIER P3600, MODIFIED

K915890 · BTT

Anesthesiology · 183d

Cleared Mar 31, 1992

AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000

K914465 · CAF

Anesthesiology · 176d

Cleared Dec 10, 1990

THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000

K903489 · BWF

Anesthesiology · 130d

Cleared Aug 28, 1989

THERA-MIST(TM) NEBULIZER, MODEL 30000

K893942 · CAF

Anesthesiology · 89d

Cleared Aug 28, 1989

THERA-MIST HUMIDIFIER

K894000 · BTT

Anesthesiology · 84d

Cleared Mar 31, 1988

AERO-MIST NEBULIZER HEATER

K880473 · CAF

Anesthesiology · 56d

Pegasus Research Corp. - FDA 510(k) Cleared Devices

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