510(k) K021385

ATAC PAK BUN REAGENT by Elan Diagnostics — Product Code CDQ

K021385 is an FDA 510(k) premarket notification submitted by Elan Diagnostics for the device "ATAC PAK BUN REAGENT". The FDA issued a decision of Substantially Equivalent on July 12, 2002. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Elan Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 2002
Date Received
May 2, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type