510(k) K790829
K790829 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "EMIT GENTAMICIN ASSAY". The FDA issued a decision of Substantially Equivalent on May 15, 1979. The device falls under product code DJB (Radioimmunoassay, Gentamicin (125-I), Second Antibody Sep.), a Class II device regulated under 21 CFR 862.3450. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 15, 1979
- Date Received
- April 30, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Gentamicin (125-I), Second Antibody Sep.
- Device Class
- Class II
- Regulation Number
- 862.3450
- Review Panel
- TX
- Submission Type