510(k) K981306

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

K981306 is an FDA 510(k) premarket notification submitted by Diamedix Corp. for the device "DIAMEDIX IS-HSV 1 & 2 IGG TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on September 29, 1998. 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
September 29, 1998
Date Received
April 10, 1998
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