Medical Device Manufacturer · US , Beaverton , OR

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

7 submissions · 7 cleared · Since 2001
7
Total
7
Cleared
0
Denied

Welch Allyn Protocol, Inc. has 7 FDA 510(k) cleared medical devices. Based in Beaverton, US.

Historical record: 7 cleared submissions from 2001 to 2007. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Welch Allyn Protocol, Inc.
7 devices
1-7 of 7
Cleared Mar 23, 2007
LINK TO ACUITY CLINICIAN NOTIFIER
K070204 · MSX
Cardiovascular · 60d
Cleared Dec 04, 2006
MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 )
K063419 · MWI
Cardiovascular · 21d
Cleared Mar 01, 2004
VITAL SIGNS MONITOR, PROPAQ LT
K033378 · MWI
Cardiovascular · 131d
Cleared Aug 26, 2003
VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIES
K031740 · DQA
Anesthesiology · 83d
Cleared Aug 21, 2002
MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM
K022453 · DSI
Cardiovascular · 26d
Cleared Jul 23, 2002
MICROPAQ, MODELS 402, 404
K021681 · DRT
Cardiovascular · 62d
Cleared Aug 20, 2001
PROPAQ ENCORE MODELS 202, 204, 206
K012451 · DRT
Cardiovascular · 19d
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