FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SURGICAL CLIPPER
K Number: K910524
·
Decision Mar 28, 1991
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
3
Applicant Total
505
Review Days
49
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Basic Information
- Device Name
- SURGICAL CLIPPER
- K Number
- K910524
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Baxter Healthcare Corp
- Date Received
- February 7, 1991
- Decision Date
- March 28, 1991
- Product Code
- LWK
- 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 |
|---|---|---|---|
| LWK | Razor, Surgical | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LWK), ordered by most recent decision date.
3M(TM) SURGICAL SLIPPER, 9660 SERIES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGICAL PREP RAZOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGICAL PREP RAZOR, STRAIGHT TYPE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
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