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

K SERIES CPAP SYSTEMS

K Number: K131702 · Decision Dec 6, 2013
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
6
Review Days
178

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Basic Information

Device Name
K SERIES CPAP SYSTEMS
K Number
K131702
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Curative Medical, Inc.
Date Received
June 11, 2013
Decision Date
December 6, 2013
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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K Number Device Name
K141354 NAVAJO PTA BALLOON DILATATION CATHETER
K130828 K SERIES CPAP SYSTEMS
K130663 BESTFIT2 NASAL MASK
K123897 K SERIES CPAP SYSTEMS
K120285 K SERIES CPAP SYSTEM WITH HEATED HUMIDIFER