510(k) K053061
K053061 is an FDA 510(k) premarket notification submitted by Dade Behring, Inc. for the device "EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY". The FDA issued a decision of Substantially Equivalent on February 6, 2006. The device falls under product code MKW (Cyclosporine), a Class II device regulated under 21 CFR 862.1235. Dade Behring, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 6, 2006
- Date Received
- October 31, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cyclosporine
- Device Class
- Class II
- Regulation Number
- 862.1235
- Review Panel
- TX
- Submission Type