510(k) K842786

DYNA-LYTE 2000 by Abbott Diagnostics — Product Code CEM

K842786 is an FDA 510(k) premarket notification submitted by Abbott Diagnostics for the device "DYNA-LYTE 2000". The FDA issued a decision of Substantially Equivalent on September 14, 1984. The device falls under product code CEM (Electrode, Ion Specific, Potassium), a Class II device regulated under 21 CFR 862.1600. Abbott Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1984
Date Received
May 22, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Ion Specific, Potassium
Device Class
Class II
Regulation Number
862.1600
Review Panel
CH
Submission Type