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

LIQUID OXYGEN STORAGE SUBSYSTEM

K Number: K941819 · Decision May 23, 1994
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
54
Applicant Total
26
Review Days
40

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Basic Information

Device Name
LIQUID OXYGEN STORAGE SUBSYSTEM
K Number
K941819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5655
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hogan & Hartson
Date Received
April 13, 1994
Decision Date
May 23, 1994
Product Code
BYJ
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
BYJ Unit, Liquid-Oxygen, Portable

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K946216 CARDIOLIPIN A EIA TEST SYSTEM
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