510(k) K904854

RUBEOLA IGG ELISA TEST by Gull Laboratories, Inc. — Product Code LJB

K904854 is an FDA 510(k) premarket notification submitted by Gull Laboratories, Inc. for the device "RUBEOLA IGG ELISA TEST". The FDA issued a decision of Substantially Equivalent on December 4, 1990. The device falls under product code LJB (Enzyme Linked Immunoabsorbent Assay, Rubeola Igg), a Class I device regulated under 21 CFR 866.3520. Gull Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 4, 1990
Date Received
October 29, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Rubeola Igg
Device Class
Class I
Regulation Number
866.3520
Review Panel
MI
Submission Type

The qualitative detection of measles specific IgG antibodies in serum or plasma.