510(k) K920300

B2-MICROGLOBULIN RADIOIMMUNOASSAY by Nichols Institute — Product Code JZG

K920300 is an FDA 510(k) premarket notification submitted by Nichols Institute for the device "B2-MICROGLOBULIN RADIOIMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on March 17, 1992. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Nichols Institute has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 17, 1992
Date Received
January 22, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Beta-2-Microglobulin Immunological
Device Class
Class II
Regulation Number
866.5630
Review Panel
IM
Submission Type