FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BEAVERS' DENTAL DIAMOND INSTRUMENTS
K Number: K880179
·
Decision Mar 9, 1988
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
20
Applicant Total
3
Review Days
56
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Basic Information
- Device Name
- BEAVERS' DENTAL DIAMOND INSTRUMENTS
- K Number
- K880179
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4535
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Beavers Dental, Div. Sybron Canada, Ltd.
- Date Received
- January 13, 1988
- Decision Date
- March 9, 1988
- Product Code
- DZP
- 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 |
|---|---|---|---|
| DZP | Instrument, Diamond, Dental | FDA class 1 | Dental |
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