510(k) K905787

VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST by Vitek Systems, Inc. — Product Code LJC

K905787 is an FDA 510(k) premarket notification submitted by Vitek Systems, Inc. for the device "VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST". The FDA issued a decision of Substantially Equivalent on April 29, 1991. The device falls under product code LJC (Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)), a Class I device regulated under 21 CFR 866.3120. Vitek Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1991
Date Received
December 27, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)
Device Class
Class I
Regulation Number
866.3120
Review Panel
MI
Submission Type