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

SPACELABS MEDICAL WORKSTATION

K Number: K860834 · Decision Apr 29, 1986
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
46
Review Days
55

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Basic Information

Device Name
SPACELABS MEDICAL WORKSTATION
K Number
K860834
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Spacelabs, Inc.
Date Received
March 5, 1986
Decision Date
April 29, 1986
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DSI), ordered by most recent decision date.

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Other Clearances by Spacelabs, Inc.

K Number Device Name
K954962 SPACELABS MEDICAL MULTIGAS ANALYZER
K951605 SPACELABS MEDICAL CASEMASTER INFORMATION MANAGEMENT SYSTEM
K950779 HEART RATE VARIABILITY SOFTWARE OPTION
K941165 COMET CAPNOGRAPH MODULE
K923788 SPACE LABS MODEL 90560
K912742 ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
K913038 SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION
K905065 DEFIBRILLATOR LEAD ADAPTER
K910029 PATIENT CARE MANAGEMENT SYSTEM MODIFICATION
K896903 FIRST MEDIC MODEL 510
Search all 46 clearances from Spacelabs, Inc. →