510(k) K833931

UREA NITROGEN-UV by Seragen Diagnostics, Inc. — Product Code CDQ

K833931 is an FDA 510(k) premarket notification submitted by Seragen Diagnostics, Inc. for the device "UREA NITROGEN-UV". The FDA issued a decision of Substantially Equivalent on January 13, 1984. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Seragen Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 13, 1984
Date Received
November 14, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type