510(k) K833984
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 4, 1984
- Date Received
- November 17, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Anti-Dna Indirect Immunofluorescent Solid Phase
- Device Class
- Class II
- Regulation Number
- 866.5100
- Review Panel
- IM
- Submission Type