FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SAW BLADE
K Number: K933298
·
Decision Aug 9, 1993
Classifications
1
FEI Numbers
304
Registration Numbers
304
Same Product Code
26
Applicant Total
3
Review Days
33
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Basic Information
- Device Name
- SAW BLADE
- K Number
- K933298
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4820
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Omega Surgical Instruments, Inc.
- Date Received
- July 7, 1993
- Decision Date
- August 9, 1993
- Product Code
- GFA
- 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 |
|---|---|---|---|
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | FDA class 1 | General, Plastic Surgery |
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