510(k) K820188

PHENOBARBITAL ASSAY by Syva Co. — Product Code LET

K820188 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "PHENOBARBITAL ASSAY". The FDA issued a decision of Substantially Equivalent on February 5, 1982. The device falls under product code LET (Fluorescent Immunoassay, Phenobarbital), a Class II device regulated under 21 CFR 862.3660. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 1982
Date Received
January 25, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay, Phenobarbital
Device Class
Class II
Regulation Number
862.3660
Review Panel
TX
Submission Type