510(k) K810261

EUROCHIMA UREA NITROGEN by Volu Sol Medical Industries — Product Code CDL

K810261 is an FDA 510(k) premarket notification submitted by Volu Sol Medical Industries for the device "EUROCHIMA UREA NITROGEN". The FDA issued a decision of Substantially Equivalent on February 10, 1981. The device falls under product code CDL (Berthelot Indophenol, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Volu Sol Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 10, 1981
Date Received
January 30, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Berthelot Indophenol, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type