510(k) K010878

MODIFICATION TO IMMULITE HERPES I & II IGG, MODEL L2KHS2 & L2KHS6 by Diagnostic Products Corp. — Product Code LGC

K010878 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "MODIFICATION TO IMMULITE HERPES I & II IGG, MODEL L2KHS2 & L2KHS6". The FDA issued a decision of Substantially Equivalent on April 18, 2001. 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. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 18, 2001
Date Received
March 19, 2001
Clearance Type
Special
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