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

CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L

K Number: K101154 · Decision Mar 28, 2011
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
18
Review Days
339

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Basic Information

Device Name
CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L
K Number
K101154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5440
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Airsep Corp.
Date Received
April 23, 2010
Decision Date
March 28, 2011
Product Code
CAW
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
CAW Generator, Oxygen, Portable

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K992283 ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
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