510(k) K904893

FIAX LYME M TEST KIT by Whittaker Bioproducts, Inc. — Product Code LSR

K904893 is an FDA 510(k) premarket notification submitted by Whittaker Bioproducts, Inc. for the device "FIAX LYME M TEST KIT". The FDA issued a decision of Substantially Equivalent on October 16, 1991. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Whittaker Bioproducts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 16, 1991
Date Received
October 30, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Borrelia Serological Reagent
Device Class
Class II
Regulation Number
866.3830
Review Panel
MI
Submission Type