510(k) K922675

PROSPECT GIARDIA CONTROLS by Alexon, Inc. — Product Code MHI

K922675 is an FDA 510(k) premarket notification submitted by Alexon, Inc. for the device "PROSPECT GIARDIA CONTROLS". The FDA issued a decision of Substantially Equivalent on September 11, 1992. 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 11, 1992
Date Received
June 4, 1992
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