510(k) K955627

VIDAS CHLAMYDIA BLOCKING ASSAY by Biomerieux Vitek, Inc. — Product Code LJC

K955627 is an FDA 510(k) premarket notification submitted by Biomerieux Vitek, Inc. for the device "VIDAS CHLAMYDIA BLOCKING ASSAY". The FDA issued a decision of Substantially Equivalent on October 7, 1996. The device falls under product code LJC (Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)), a Class I device regulated under 21 CFR 866.3120. Biomerieux Vitek, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 1996
Date Received
December 11, 1995
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