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

SPACELABS SERIES 90700 PATIENT MONITORS

K Number: K862951 · Decision Sep 23, 1986
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
46
Review Days
49

Basic Information

Device Name
SPACELABS SERIES 90700 PATIENT MONITORS
K Number
K862951
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SPACELABS, INC.
Date Received
August 5, 1986
Decision Date
September 23, 1986
Product Code
DPS
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
DPS Electrocardiograph

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K Number Device Name
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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
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