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

CPAP Cannulaide

K Number: K143700 · Decision Aug 5, 2015
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
48
Review Days
224

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Basic Information

Device Name
CPAP Cannulaide
K Number
K143700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Salter Labs
Date Received
December 24, 2014
Decision Date
August 5, 2015
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

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K142416 Luma Wrap
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K040202 SALTER LABS CPAP HIGH FLOW CANNULA SYSTEM
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K992285 SALTER AIRE COMPRESSOR
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