930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES
FDA 510(k) clearance K851718 · decided 1985-07-02
Clearance details
- K-number
- K851718
- Device name
- 930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES
- Applicant
- Artiberia
- Decision
- Substantially Equivalent
- Date received
- 1985-04-25
- Decision date
- 1985-07-02
- Days to decision
- 68 days
- Clearance type
- Traditional
- Product code
- EMK
- Device class
- 1
- Regulation number
- 872.4565
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- San Antonio, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.