FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PORTABLE OXYGEN SYSTEM

K Number: K830844 · Decision May 27, 1983
Classifications
1
FEI Numbers
113
Registration Numbers
114
Same Product Code
54
Applicant Total
110
Review Days
71

Basic Information

Device Name
PORTABLE OXYGEN SYSTEM
K Number
K830844
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.2700
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
PURITAN BENNETT CORP.
Date Received
March 17, 1983
Decision Date
May 27, 1983
Product Code
CAN
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
CAN Regulator, Pressure, Gas Cylinder

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