510(k) K781885

SERUM, BLOOD UREA NITIOGEN by Fisher Scientific Co., LLC — Product Code CDW

K781885 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "SERUM, BLOOD UREA NITIOGEN". The FDA issued a decision of Substantially Equivalent on December 20, 1978. The device falls under product code CDW (Diacetyl-Monoxime, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 20, 1978
Date Received
November 7, 1978
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