FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FORCEPS
K Number: K904723
·
Decision Jul 26, 1991
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
4
Review Days
282
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Basic Information
- Device Name
- FORCEPS
- K Number
- K904723
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Minto Research & Development, Inc.
- Date Received
- October 17, 1990
- Decision Date
- July 26, 1991
- Product Code
- GEN
- 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 |
|---|---|---|---|
| GEN | Forceps, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
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