510(k) K820285

SYVA ADVANCE SYST. EMIT-AMD GENT. ASSAY by Syva Co. — Product Code LCQ

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