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

SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION

K Number: K913038 · Decision Oct 4, 1991
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
46
Review Days
87

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Basic Information

Device Name
SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION
K Number
K913038
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Spacelabs, Inc.
Date Received
July 9, 1991
Decision Date
October 4, 1991
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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K941165 COMET CAPNOGRAPH MODULE
K923788 SPACE LABS MODEL 90560
K912742 ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
K905065 DEFIBRILLATOR LEAD ADAPTER
K910029 PATIENT CARE MANAGEMENT SYSTEM MODIFICATION
K896903 FIRST MEDIC MODEL 510
K904318 LOCAL REPORT GENERATOR
Search all 46 clearances from Spacelabs, Inc. →