510(k) K802573
K802573 is an FDA 510(k) premarket notification submitted by Worthington Diagnostic Systems for the device "SERUM T4 BY ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on November 24, 1980. The device falls under product code CDX (Radioimmunoassay, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Worthington Diagnostic Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 24, 1980
- Date Received
- October 17, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Total Thyroxine
- Device Class
- Class II
- Regulation Number
- 862.1700
- Review Panel
- CH
- Submission Type