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

SPACELABS MEDICAL MULTIGAS ANALYZER

K Number: K954962 · Decision May 31, 1996
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
4
Applicant Total
46
Review Days
214

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Basic Information

Device Name
SPACELABS MEDICAL MULTIGAS ANALYZER
K Number
K954962
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1700
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Spacelabs, Inc.
Date Received
October 30, 1995
Decision Date
May 31, 1996
Product Code
CBR
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
CBR Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.)

Similar 510(k) Clearances

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

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Other Clearances by Spacelabs, Inc.

K Number Device Name
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
K904318 LOCAL REPORT GENERATOR
Search all 46 clearances from Spacelabs, Inc. →