510(k) K033780

MODIFICATION TO SERAQUEST VCA IGM by Quest Intl., Inc. — Product Code LJN

K033780 is an FDA 510(k) premarket notification submitted by Quest Intl., Inc. for the device "MODIFICATION TO SERAQUEST VCA IGM". The FDA issued a decision of Substantially Equivalent on January 15, 2004. The device falls under product code LJN (Antibody Igm, If, Epstein-Barr Virus), a Class I device regulated under 21 CFR 866.3235. Quest Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 15, 2004
Date Received
December 4, 2003
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antibody Igm, If, Epstein-Barr Virus
Device Class
Class I
Regulation Number
866.3235
Review Panel
MI
Submission Type