510(k) K942098

PROSPECT GIARDIA by Alexon, Inc. — Product Code MHI

K942098 is an FDA 510(k) premarket notification submitted by Alexon, Inc. for the device "PROSPECT GIARDIA". The FDA issued a decision of Substantially Equivalent on September 9, 1994. 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
September 9, 1994
Date Received
April 14, 1994
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