510(k) K930451

PROSPEC T GIARDIA MICROTITER ASSAY by Alexon, Inc. — Product Code MHI

K930451 is an FDA 510(k) premarket notification submitted by Alexon, Inc. for the device "PROSPEC T GIARDIA MICROTITER ASSAY". The FDA issued a decision of Substantially Equivalent on April 21, 1993. The device falls under product code MHI (Giardia Spp.), a Class II device regulated under 21 CFR 866.3220. Alexon, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 1993
Date Received
January 27, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Giardia Spp.
Device Class
Class II
Regulation Number
866.3220
Review Panel
MI
Submission Type