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

MONITOR, OXYCHEK OXYGEN

K Number: K782114 · Decision Jan 18, 1979
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
51
Review Days
29

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Basic Information

Device Name
MONITOR, OXYCHEK OXYGEN
K Number
K782114
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Critikon Company, LLC
Date Received
December 20, 1978
Decision Date
January 18, 1979
Product Code
CCL
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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

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K915697 CRITIKON VITAL SIGNS MODULE
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