510(k) K860419

UREA NITROGEN REAGENT SET by Sterling Diagnostics, Inc. — Product Code CDW

K860419 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "UREA NITROGEN REAGENT SET". The FDA issued a decision of Substantially Equivalent on February 11, 1986. The device falls under product code CDW (Diacetyl-Monoxime, 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
February 11, 1986
Date Received
February 4, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Diacetyl-Monoxime, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type