510(k) K862210

UREA NITROGEN (GLDH) REAGENT SET (UV) by Sterling Diagnostics, Inc. — Product Code CDQ

K862210 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "UREA NITROGEN (GLDH) REAGENT SET (UV)". The FDA issued a decision of Substantially Equivalent on July 1, 1986. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 1, 1986
Date Received
June 10, 1986
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