510(k) K935014

ACTIVE DEHYDROEPIANDROSTERONE (DHEA)(DSL 9000) by Diagnostic Systems Laboratories, Inc. — Product Code JKC

K935014 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "ACTIVE DEHYDROEPIANDROSTERONE (DHEA)(DSL 9000)". The FDA issued a decision of Substantially Equivalent on May 9, 1994. The device falls under product code JKC (Radioimmunoassay, Dehydroepiandrosterone (Free And Sulfate)), a Class I device regulated under 21 CFR 862.1245. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1994
Date Received
October 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Dehydroepiandrosterone (Free And Sulfate)
Device Class
Class I
Regulation Number
862.1245
Review Panel
CH
Submission Type