510(k) K032692
K032692 is an FDA 510(k) premarket notification submitted by Dako A/S for the device "DAKOCYTOMATION BETA-2-MICROGLOBULIN KIT, CODE NO. OA 368". The FDA issued a decision of Substantially Equivalent on January 22, 2004. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Dako A/S has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 22, 2004
- Date Received
- September 2, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, Beta-2-Microglobulin Immunological
- Device Class
- Class II
- Regulation Number
- 866.5630
- Review Panel
- IM
- Submission Type