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

3B RESMART CPAP AND AUTO CPAP SYSTEMS, BMC RESMART CPAP AND AUTO CPAP SYSTEMS

K Number: K131707 · Decision Aug 22, 2013
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
10
Review Days
72

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Basic Information

Device Name
3B RESMART CPAP AND AUTO CPAP SYSTEMS, BMC RESMART CPAP AND AUTO CPAP SYSTEMS
K Number
K131707
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3B Medical, Inc.
Date Received
June 11, 2013
Decision Date
August 22, 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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K141770 LUNA CPAP AND AUTO-CPAP SYSTEM
K133769 3B RESMART BPAP 25A, BMC RESMART BPAP 25A
K131901 IVOLVE NASAL MASK, IVOLVE FULL FACE MASK, IVOLVE N2
K132967 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP