510(k) K801727

DATA-ZYME UREA NITROGEN, COLORIMETRIC by Data Medical Associates, Inc. — Product Code CDL

K801727 is an FDA 510(k) premarket notification submitted by Data Medical Associates, Inc. for the device "DATA-ZYME UREA NITROGEN, COLORIMETRIC". The FDA issued a decision of Substantially Equivalent on September 9, 1980. The device falls under product code CDL (Berthelot Indophenol, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Data Medical Associates, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 1980
Date Received
July 24, 1980
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