510(k) K904854
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.