Medical Device Manufacturer · US , Colton , CA

Pulmonetic Systems, Inc. - FDA 510(k) Cleared Devices

12 submissions · 11 cleared · Since 1998

Recent clearances: PULMONETIC SYSTEMS LTV 1200 MR CONDITIONAL VENTILATOR, PALMTOP VENTILATOR, MODELS PTV-8, PTV-10, LTV 1200 VENTILATOR

View 12 510(k) Devices ↓

Total

Cleared

Denied

Pulmonetic Systems, Inc. has 11 FDA 510(k) cleared anesthesiology devices. Based in Colton, US.

Historical record: 11 cleared submissions from 1998 to 2009.

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

Pulmonetic Systems, Inc. is one of 18330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pulmonetic Systems, Inc.

12 devices

1-12 of 12

Cleared Mar 18, 2009

PULMONETIC SYSTEMS LTV 1200 MR CONDITIONAL VENTILATOR

K083688 · CBK

Anesthesiology · 96d

Cleared Aug 01, 2007

PALMTOP VENTILATOR, MODELS PTV-8, PTV-10

K070594 · CBK

Anesthesiology · 152d

AUTOMOBILE LIGHTER POWER CORD

MODIFICATION TO LTV 1000 VENTILATOR/BREATHING CIRCUITS

K040790 · CBK

Anesthesiology · 66d

Cleared Apr 29, 2004

MODIFICATION TO LTV 1000 VENTILATOR

MODIFICATION TO LAP TOP VENTILATOR (LTV)

K010608 · CBK

Anesthesiology · 19d

Cleared Oct 11, 2000

VENTILATOR, CONTINUOUS (RESPIRATOR), MODEL LTV 1000

Anesthesiology · 150d

Cleared Oct 30, 1998

LTV 1000 VENTILATOR

K981371 · CBK

Anesthesiology · 197d

Pulmonetic Systems, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Pulmonetic Systems, Inc.

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