510(k) K872056

MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST by Boots-Celltech Diagnostics, Inc. — Product Code LJC

K872056 is an FDA 510(k) premarket notification submitted by Boots-Celltech Diagnostics, Inc. for the device "MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST". The FDA issued a decision of Substantially Equivalent on June 15, 1987. 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
June 15, 1987
Date Received
May 28, 1987
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