The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Calcimol Lc.
| Device ID | K924182 |
| 510k Number | K924182 |
| Device Name: | CALCIMOL LC |
| Classification | Liner, Cavity, Calcium Hydroxide |
| Applicant | VOCO GMBH C/ONDA RESOURCES 790 WASHINGTON STREET, STE 301 Denver, CO 80203 |
| Contact | Gail E Gillenwater |
| Correspondent | Gail E Gillenwater VOCO GMBH C/ONDA RESOURCES 790 WASHINGTON STREET, STE 301 Denver, CO 80203 |
| Product Code | EJK |
| CFR Regulation Number | 872.3250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-19 |
| Decision Date | 1992-10-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| E22113071 | K924182 | 000 |