Medical Device Manufacturer · US , Beaverton , OR

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

15 submissions · 14 cleared · Since 1988

Total

Cleared

Denied

Protocol Systems, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Beaverton, US.

Historical record: 14 cleared submissions from 1988 to 2000.

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

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

15 devices

1-12 of 15

Cleared Nov 21, 2000

MICROPAQ, MODELS 402 AND 404

K002725 · DRT

Cardiovascular · 82d

Cleared Nov 07, 1997

ACUITY CENTRAL STATION

K972121 · MLD

Cardiovascular · 155d

Cleared Feb 02, 1996

PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE...

K951246 · FLS

Anesthesiology · 319d

Cleared May 10, 1995

PROPAQ 200 MONITOR

K945071 · DRT

Cardiovascular · 208d

Cleared Dec 05, 1994

MODEL ACUITY CENTRAL STATION

K935846 · DSI

Cardiovascular · 362d

Cleared Sep 01, 1994

PROPAQ ECG TELEMETRY OPTION

K934711 · DRG

Cardiovascular · 335d

Cleared Mar 23, 1993

PROPAQ MONITORS, MODIFICATION

K921497 · CCK

Anesthesiology · 377d

Cleared Jan 10, 1992

PROPAQ 102,104,106,102EL,104EL,&106EL

K914838 · MHX

Cardiovascular · 77d

Cleared Oct 16, 1991

MODEL 100 CENTRAL STATION

K913193 · DQK

Cardiovascular · 90d

Cleared May 08, 1991

PROPAQ 102EL, 104EL AND 106EL

K910882 · DRT

Cardiovascular · 68d

Cleared Apr 12, 1991

PROPAQ 102, 104 AND 106

Anesthesiology · 123d

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

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