FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UTILITY CLAMP
K Number: K881084
·
Decision Mar 25, 1988
Classifications
1
FEI Numbers
270
Registration Numbers
270
Same Product Code
31
Applicant Total
4
Review Days
11
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Basic Information
- Device Name
- UTILITY CLAMP
- K Number
- K881084
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Med-Dex Intl.
- Date Received
- March 14, 1988
- Decision Date
- March 25, 1988
- Product Code
- GDJ
- 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 |
|---|---|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
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