510(k) K884201
K884201 is an FDA 510(k) premarket notification submitted by Cyberfluor, Inc. for the device "FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on December 14, 1988. The device falls under product code CEE (Radioimmunoassay, Thyroxine-Binding Globulin), a Class II device regulated under 21 CFR 862.1685. Cyberfluor, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 14, 1988
- Date Received
- October 6, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Thyroxine-Binding Globulin
- Device Class
- Class II
- Regulation Number
- 862.1685
- Review Panel
- CH
- Submission Type