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

SPACELABS P.C. CARDIAC OUTPUT/PRESSURE MODULE

K Number: K860689 · Decision Jul 30, 1986
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
76
Applicant Total
46
Review Days
155

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Basic Information

Device Name
SPACELABS P.C. CARDIAC OUTPUT/PRESSURE MODULE
K Number
K860689
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1110
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Spacelabs, Inc.
Date Received
February 25, 1986
Decision Date
July 30, 1986
Product Code
DSK
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
DSK Computer, Blood-Pressure

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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. →