FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AURA CPAP PATIENT INTERFACE
K Number: K042130
·
Decision Sep 8, 2004
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
4
Review Days
33
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Basic Information
- Device Name
- AURA CPAP PATIENT INTERFACE
- K Number
- K042130
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 868.5905
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Aeiomed, Inc.
- Date Received
- August 6, 2004
- Decision Date
- September 8, 2004
- 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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