510(k) K932659

MULTI LEVEL CONTROL FOR CKMB ISOENSYME IN SYRUM by More Diagnostics — Product Code JJX

K932659 is an FDA 510(k) premarket notification submitted by More Diagnostics for the device "MULTI LEVEL CONTROL FOR CKMB ISOENSYME IN SYRUM". The FDA issued a decision of Substantially Equivalent on July 28, 1993. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. More Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 1993
Date Received
June 2, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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