The following data is part of a premarket notification filed by Sinmed Bv with the FDA for Sinmed Positioning Devices.
| Device ID | K060737 |
| 510k Number | K060737 |
| Device Name: | SINMED POSITIONING DEVICES |
| Classification | Accelerator, Linear, Medical |
| Applicant | SINMED BV 6,PASTEURSTRAAT Reeuwijk, NL 2811 Dx |
| Contact | Caroline De Keijzer |
| Correspondent | J.a. Van Vugt KEMA QUALITY B.V. 4377 COUNTY LINE ROAD Chalfont, PA 18914 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2006-03-20 |
| Decision Date | 2006-03-31 |
| Summary: | summary |