FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AG-PLUS, MODEL 91210
K Number: K060404
·
Decision Jun 22, 2006
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
4
Review Days
127
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Basic Information
- Device Name
- AG-PLUS, MODEL 91210
- K Number
- K060404
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medel S.P.A.
- Date Received
- February 15, 2006
- Decision Date
- June 22, 2006
- Product Code
- CAF
- 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 |
|---|---|---|---|
| CAF | Nebulizer (Direct Patient Interface) | FDA class 2 | Anesthesiology |
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