Welch Allyn Protocol, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Welch Allyn Protocol, Inc. - FDA 510(k) Cleared Devices
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
Cleared
Mar 23, 2007
LINK TO ACUITY CLINICIAN NOTIFIER
Cardiovascular
60d
Cleared
Dec 04, 2006
MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 )
Cardiovascular
21d
Cleared
Mar 01, 2004
VITAL SIGNS MONITOR, PROPAQ LT
Cardiovascular
131d
Cleared
Aug 26, 2003
VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIES
Anesthesiology
83d
Cleared
Aug 21, 2002
MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM
Cardiovascular
26d
Cleared
Jul 23, 2002
MICROPAQ, MODELS 402, 404
Cardiovascular
62d
Cleared
Aug 20, 2001
PROPAQ ENCORE MODELS 202, 204, 206
Cardiovascular
19d