510(k) K851239

ACTIVE DHEA-SULFATE DSL3500 by Diagnostic Systems Laboratories, Inc. — Product Code JKC

K851239 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "ACTIVE DHEA-SULFATE DSL3500". The FDA issued a decision of Substantially Equivalent on April 25, 1985. 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
April 25, 1985
Date Received
March 27, 1985
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