510(k) K932980
K932980 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "TOTAL T4 FPIA REAGENT SET/CALIBRATOR #T-1039,T-116". The FDA issued a decision of Substantially Equivalent on October 18, 1993. The device falls under product code CDX (Radioimmunoassay, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 18, 1993
- Date Received
- June 17, 1993
- 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