FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AURA-PSG
K Number: K050425
·
Decision Oct 20, 2005
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
63
Applicant Total
13
Review Days
244
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Basic Information
- Device Name
- AURA-PSG
- K Number
- K050425
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Astro-Med, Inc.
- Date Received
- February 18, 2005
- Decision Date
- October 20, 2005
- Product Code
- OLV
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| OLV | Standard Polysomnograph With Electroencephalograph | FDA class 2 | Neurology |
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