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

FDA 510(k) Regulatory Record - Welch Allyn Protocol, Inc. Cardiovascular ✕

6 devices

1-6 of 6

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 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