FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FORCEPS, STYLE #849
K Number: K771522
·
Decision Aug 16, 1977
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
7
Applicant Total
41
Review Days
8
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Basic Information
- Device Name
- FORCEPS, STYLE #849
- K Number
- K771522
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Premier Dental Products Co.
- Date Received
- August 8, 1977
- Decision Date
- August 16, 1977
- Product Code
- EMH
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| EMH | Forceps, Rongeur, Surgical | FDA class 1 | Dental |
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