510(k) K921205

DSL ACTIVE ALDOSTERONE (DSL 8600) by Diagnostic Systems Laboratories, Inc. — Product Code CJM

K921205 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL ACTIVE ALDOSTERONE (DSL 8600)". The FDA issued a decision of Substantially Equivalent on July 10, 1992. The device falls under product code CJM (Radioimmunoassay, Aldosterone), a Class II device regulated under 21 CFR 862.1045. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 10, 1992
Date Received
March 12, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Aldosterone
Device Class
Class II
Regulation Number
862.1045
Review Panel
CH
Submission Type