510(k) K002262

DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM by Diamedix Corp. — Product Code LGC

K002262 is an FDA 510(k) premarket notification submitted by Diamedix Corp. for the device "DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on November 28, 2000. 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. Diamedix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 28, 2000
Date Received
July 25, 2000
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