510(k) K904083

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

K904083 is an FDA 510(k) premarket notification submitted by Gull Laboratories, Inc. for the device "RUBEOLA IGM ELISA TEST". The FDA issued a decision of Substantially Equivalent on January 3, 1991. 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
January 3, 1991
Date Received
September 5, 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.