Medical Device Manufacturer · US , Bothell , WA

Data Critical Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1997

Total

Cleared

Denied

Data Critical Corp. has 9 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 9 cleared submissions from 1997 to 2001. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Data Critical Corp. Filter by specialty or product code using the sidebar.

Data Critical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Data Critical Corp.

9 devices

1-9 of 9

Cleared Oct 19, 2001

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

K013156 · MSX

Cardiovascular · 28d

Cleared Jul 24, 2001

MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

K011999 · MSX

Cardiovascular · 27d

Cleared Jul 24, 2001

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

K012005 · MSX

Cardiovascular · 27d

Cleared Apr 05, 2001

ALARMVIEW WIRELESS DATA NETWORK SYSTEM

K010912 · MSX

Cardiovascular · 9d

Cleared Mar 07, 2001

FLEXVIEW CLINICAL MONITORING SYSTEM

Cardiovascular · 224d

Cleared Mar 31, 1998

CARDIO-PAGER SYSTEM

K973527 · MSX

Cardiovascular · 194d

Cleared Dec 04, 1997

RHYTHMSTAT XL

K971650 · DXH

Cardiovascular · 212d

Data Critical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Data Critical Corp.

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