510(k) K802160

BUN COLOR REAGENT & BUN ACID USED by Panmed, Inc. — Product Code CDW

K802160 is an FDA 510(k) premarket notification submitted by Panmed, Inc. for the device "BUN COLOR REAGENT & BUN ACID USED". The FDA issued a decision of Substantially Equivalent on October 10, 1980. The device falls under product code CDW (Diacetyl-Monoxime, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Panmed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 10, 1980
Date Received
September 8, 1980
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