510(k) K931147

PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATION by Alexon, Inc. — Product Code MHI

K931147 is an FDA 510(k) premarket notification submitted by Alexon, Inc. for the device "PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATION". The FDA issued a decision of Substantially Equivalent on May 13, 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
May 13, 1993
Date Received
March 5, 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