FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SNIFF POSITION PILLOWS/POPITZ PILLOWS
K Number: K023010
·
Decision Oct 1, 2002
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
5
Applicant Total
1
Review Days
22
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Basic Information
- Device Name
- SNIFF POSITION PILLOWS/POPITZ PILLOWS
- K Number
- K023010
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 872.5570
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Aeolus International Corporation
- Date Received
- September 9, 2002
- Decision Date
- October 1, 2002
- Product Code
- MYB
- Advisory Committee
- Dental
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| MYB | Pillow, Cervical (For Mild Sleep Apnea) | FDA class 2 | Dental |
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