510(k) K992430

CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 by Medical Analysis Systems, Inc. — Product Code JJT

K992430 is an FDA 510(k) premarket notification submitted by Medical Analysis Systems, Inc. for the device "CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3". The FDA issued a decision of Substantially Equivalent on August 30, 1999. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Medical Analysis Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1999
Date Received
July 21, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type