510(k) K880799

MODIFIED IDEIA CHLAMYDIA TEST by Boots-Celltech Diagnostics, Inc. — Product Code LJC

K880799 is an FDA 510(k) premarket notification submitted by Boots-Celltech Diagnostics, Inc. for the device "MODIFIED IDEIA CHLAMYDIA TEST". The FDA issued a decision of Substantially Equivalent on December 8, 1988. The device falls under product code LJC (Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)), a Class I device regulated under 21 CFR 866.3120. Boots-Celltech Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 8, 1988
Date Received
February 29, 1988
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