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

SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION

K Number: K101850 · Decision Mar 2, 2011
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
9
Review Days
244

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Basic Information

Device Name
SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION
K Number
K101850
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spacelabs Healthcare, Ltd.
Date Received
July 1, 2010
Decision Date
March 2, 2011
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

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K141113 SPACELBS MODEL ON TRAK (90227) AMBULATORY BLOODY PRESSURE (ABP) NON-INVASIVE
K130207 SPACELABS HEALTHCARE CARDIOEXPRESS
K110001 SPACELABS PATHFINDER SL HOLTER ANALYZER
K103732 SPACELABS MODEL 90217A AMBULATORY BLOOD PRESSURE (ABP) MONITOR