510(k) K833984
K833984 is an FDA 510(k) premarket notification submitted by Intl. Diagnostic Technology for the device "ANTINUCLEAR ANTIBODY IMMUNOLOGICAL". The FDA issued a decision of Substantially Equivalent on January 4, 1984. The device falls under product code KTL (Anti-Dna Indirect Immunofluorescent Solid Phase), a Class II device regulated under 21 CFR 866.5100. Intl. Diagnostic Technology has at least 10 other 510(k) clearances on record.
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