FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WELCH ALLYN SPOT VITAL SIGNS LXI MODEL 45000 SERIES

K Number: K101680 · Decision Jul 9, 2010
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
111
Review Days
24

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Basic Information

Device Name
WELCH ALLYN SPOT VITAL SIGNS LXI MODEL 45000 SERIES
K Number
K101680
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welch Allyn, Inc.
Date Received
June 15, 2010
Decision Date
July 9, 2010
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

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K Number Device Name
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K212473 Welch Allyn Connex Central Station
K191013 Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry option
K181016 Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System
K171621 Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor
K142356 Connex Spot Monitor,901058 Vital Signs Monitor Core
K132807 MONITORING STATION, CONNEX(R) CENTRAL STATION (CS)
K132808 VITAL SIGNS MONITOR, CONNEX VITAL SIGNS MONITOR
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