510(k) K933314
K933314 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "RADIAS FERRITIN ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on September 8, 1993. The device falls under product code DEW (Igg, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Bio-Rad has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 1993
- Date Received
- July 7, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Igg, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- IM
- Submission Type