The following data is part of a premarket notification filed by Apollo Dental Products, Inc. with the FDA for Apollo Vs, Vt, Vr 1000/1500, Freedom Hs, Ht, Hr.
| Device ID | K883904 |
| 510k Number | K883904 |
| Device Name: | APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR |
| Classification | Unit, Operative Dental |
| Applicant | APOLLO DENTAL PRODUCTS, INC. 1206 G ST. #103 Fresno, CA 93706 |
| Contact | Edward Wisniewski |
| Correspondent | Edward Wisniewski APOLLO DENTAL PRODUCTS, INC. 1206 G ST. #103 Fresno, CA 93706 |
| Product Code | EIA |
| CFR Regulation Number | 872.6640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-15 |
| Decision Date | 1988-12-07 |