FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MICROAIRE MODEL 2600
K Number: K915670
·
Decision Mar 18, 1992
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
3
Applicant Total
3
Review Days
90
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Basic Information
- Device Name
- MICROAIRE MODEL 2600
- K Number
- K915670
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Microaire
- Date Received
- December 19, 1991
- Decision Date
- March 18, 1992
- Product Code
- GEF
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GEF | Applier, Staple, Surgical, | FDA class 1 | General, Plastic Surgery |
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