The following data is part of a premarket notification filed by Carefusion 2200 with the FDA for V. Mueller Camera Controller With Storage Cart.
Device ID | K093616 |
510k Number | K093616 |
Device Name: | V. MUELLER CAMERA CONTROLLER WITH STORAGE CART |
Classification | Endoscope Holder |
Applicant | CAREFUSION 2200 1500 WAUKEGAN ROAD Waukegan, IL 60085 |
Contact | Gina Rajterowski |
Correspondent | Gina Rajterowski CAREFUSION 2200 1500 WAUKEGAN ROAD Waukegan, IL 60085 |
Product Code | OCV |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-11-19 |
Decision Date | 2009-12-23 |
Summary: | summary |