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Welch Allyn Protocol, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K070204	LINK TO ACUITY CLINICIAN NOTIFIER	MSX	2007-03-23	View
510(k)	K063419	MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 )	MWI	2006-12-04	View
510(k)	K033378	VITAL SIGNS MONITOR, PROPAQ LT	MWI	2004-03-01	View
510(k)	K031740	VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIES	DQA	2003-08-26	View
510(k)	K022453	MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM	DSI	2002-08-21	View
510(k)	K021681	MICROPAQ, MODELS 402, 404	DRT	2002-07-23	View
510(k)	K012451	PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246	DRT	2001-08-20	View

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