510(k) K771312

BLOOD UREA NITROGEN (BUN) REAGENT by Mallinckrodt Critical Care — Product Code CDW

K771312 is an FDA 510(k) premarket notification submitted by Mallinckrodt Critical Care for the device "BLOOD UREA NITROGEN (BUN) REAGENT". The FDA issued a decision of Substantially Equivalent on August 3, 1977. The device falls under product code CDW (Diacetyl-Monoxime, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Mallinckrodt Critical Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1977
Date Received
July 18, 1977
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