510(k) K820285
K820285 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "SYVA ADVANCE SYST. EMIT-AMD GENT. ASSAY". The FDA issued a decision of Substantially Equivalent on February 18, 1982. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), 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
- February 18, 1982
- Date Received
- February 2, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorescent Immunoassay Gentamicin
- Device Class
- Class II
- Regulation Number
- 862.3450
- Review Panel
- TX
- Submission Type