FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

O_TWO CPAP SYSTEM

K Number: K112546 · Decision Dec 27, 2011
Classifications
1
FEI Numbers
71
Registration Numbers
72
Same Product Code
79
Applicant Total
8
Review Days
117

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Basic Information

Device Name
O_TWO CPAP SYSTEM
K Number
K112546
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5965
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
O-Two Medical Technologies, Inc.
Date Received
September 1, 2011
Decision Date
December 27, 2011
Product Code
BYE
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
BYE Attachment, Breathing, Positive End Expiratory Pressure

Similar 510(k) Clearances

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

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Other Clearances by O-Two Medical Technologies, Inc.

K Number Device Name
K173205 Equinox Advantage
K141595 O-TWO E700,O-TWO E600,O-TWO E500
K113687 EQUINOX RELIEVE
K093862 CAREVENT HANDHELD CPAP SYSTEM
K081330 CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR)
K051469 CAREVENT ATV+ AND CAREVENT MRI
K051889 CAREVENT CA AND DRA