510(k) K951549

EBNA IGG EIA TEST SYSTEM by Immunoprobe, Inc. — Product Code LLM

K951549 is an FDA 510(k) premarket notification submitted by Immunoprobe, Inc. for the device "EBNA IGG EIA TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on April 29, 1996. The device falls under product code LLM (Test, Antigen, Nuclear, Epstein-Barr Virus), a Class I device regulated under 21 CFR 866.3235. Immunoprobe, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1996
Date Received
April 4, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Antigen, Nuclear, Epstein-Barr Virus
Device Class
Class I
Regulation Number
866.3235
Review Panel
MI
Submission Type