510(k) K093616
K093616 is an FDA 510(k) premarket notification submitted by Carefusion 2200 for the device "V. MUELLER CAMERA CONTROLLER WITH STORAGE CART". The FDA issued a decision of Substantially Equivalent on December 23, 2009. The device falls under product code OCV (Endoscope Holder), a Class II device regulated under 21 CFR 876.1500. Carefusion 2200 has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 23, 2009
- Date Received
- November 19, 2009
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscope Holder
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
To hold endoscope in a desired position during procedures.