510(k) K973966
K973966 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "ACCESS TOTAL T3 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER". The FDA issued a decision of Substantially Equivalent on October 31, 1997. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 1997
- Date Received
- October 17, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Total Triiodothyronine
- Device Class
- Class II
- Regulation Number
- 862.1710
- Review Panel
- CH
- Submission Type