CALCIMOL
FDA 510(k) clearance K923849 · decided 1992-09-28
Clearance details
- K-number
- K923849
- Device name
- CALCIMOL
- Applicant
- Voco GmbH
- Decision
- Substantially Equivalent
- Date received
- 1992-07-31
- Decision date
- 1992-09-28
- Days to decision
- 59 days
- Clearance type
- Traditional
- Product code
- EJK
- Device class
- 2
- Regulation number
- 872.3250
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Denver, CO, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.