510(k) K971823

ACTIVE TESTOSTERONE EIA (DSL-10-4000) by Diagnostic Systems Laboratories, Inc. — Product Code CDZ

K971823 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "ACTIVE TESTOSTERONE EIA (DSL-10-4000)". The FDA issued a decision of Substantially Equivalent on June 16, 1997. The device falls under product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone), a Class I device regulated under 21 CFR 862.1680. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 16, 1997
Date Received
May 16, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Testosterones And Dihydrotestosterone
Device Class
Class I
Regulation Number
862.1680
Review Panel
CH
Submission Type