510(k) K883767

LYME DISEASE IFA (IGM) by Hillcrest Biologicals — Product Code LSR

K883767 is an FDA 510(k) premarket notification submitted by Hillcrest Biologicals for the device "LYME DISEASE IFA (IGM)". The FDA issued a decision of Substantially Equivalent on March 15, 1989. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Hillcrest Biologicals has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 15, 1989
Date Received
September 6, 1988
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