510(k) K871877

IDEIA HERPES SIMPLEX VIRUS TEST by Boots-Celltech Diagnostics, Inc. — Product Code LGC

K871877 is an FDA 510(k) premarket notification submitted by Boots-Celltech Diagnostics, Inc. for the device "IDEIA HERPES SIMPLEX VIRUS TEST". The FDA issued a decision of Substantially Equivalent on November 17, 1989. The device falls under product code LGC (Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific), a Class II device regulated under 21 CFR 866.3305. Boots-Celltech Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 17, 1989
Date Received
May 14, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific
Device Class
Class II
Regulation Number
866.3305
Review Panel
MI
Submission Type