510(k) K900704

MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA by Innotron of Oregon, Inc. — Product Code LGQ

K900704 is an FDA 510(k) premarket notification submitted by Innotron of Oregon, Inc. for the device "MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA". The FDA issued a decision of Substantially Equivalent on April 12, 1990. The device falls under product code LGQ (Fluorescence Polarization Immunoassay, Phenobarbital), a Class II device regulated under 21 CFR 862.3660. Innotron of Oregon, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 1990
Date Received
February 12, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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