510(k) K890774

GIARDEIA(TM) by Antibodies, Inc. — Product Code KHW

K890774 is an FDA 510(k) premarket notification submitted by Antibodies, Inc. for the device "GIARDEIA(TM)". The FDA issued a decision of Substantially Equivalent on April 4, 1989. The device falls under product code KHW (Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.), a Class II device regulated under 21 CFR 866.3220. Antibodies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 1989
Date Received
February 15, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
Device Class
Class II
Regulation Number
866.3220
Review Panel
MI
Submission Type