FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP
K Number: K132967
·
Decision Dec 6, 2013
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
10
Review Days
77
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Basic Information
- Device Name
- 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP
- K Number
- K132967
- 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
- September 20, 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 | Device Class | Medical Specialty |
|---|---|---|---|
| BZD | Ventilator, Non-Continuous (Respirator) | FDA class 2 | Anesthesiology |
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| K141770 | LUNA CPAP AND AUTO-CPAP SYSTEM | Apr 22, 2015 | Substantially Equivalent |
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| K131707 | 3B RESMART CPAP AND AUTO CPAP SYSTEMS, BMC RESMART CPAP AND AUTO CPAP SYSTEMS | Aug 22, 2013 | Substantially Equivalent |