510(k) K892331

ENZYMATIC UREA NITROGEN REAGENT SET by American Monitor Corp. — Product Code CDQ

K892331 is an FDA 510(k) premarket notification submitted by American Monitor Corp. for the device "ENZYMATIC UREA NITROGEN REAGENT SET". The FDA issued a decision of Substantially Equivalent on June 20, 1989. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. American Monitor Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1989
Date Received
April 5, 1989
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