The following data is part of a premarket notification filed by Sopro with the FDA for Sopro595 Intra Oral Camera.
| Device ID | K012505 |
| 510k Number | K012505 |
| Device Name: | SOPRO595 INTRA ORAL CAMERA |
| Classification | Unit, Operative Dental |
| Applicant | SOPRO PLACE ST. CHRISTOPHE LES ACCATES-LA VALENTINE Marseille, FR F-13011 |
| Contact | Pierre Montillot |
| Correspondent | Pierre Montillot SOPRO PLACE ST. CHRISTOPHE LES ACCATES-LA VALENTINE Marseille, FR F-13011 |
| Product Code | EIA |
| CFR Regulation Number | 872.6640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-08-03 |
| Decision Date | 2001-10-05 |
| Summary: | summary |