510(k) K950670

IMMULITE HERPES I AND II IGG by Diagnostic Products Corp. — Product Code LGC

K950670 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE HERPES I AND II IGG". The FDA issued a decision of Substantially Equivalent on June 21, 1996. 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
June 21, 1996
Date Received
February 13, 1995
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