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 |