510(k) K854673

DSL ANDROSTENEDIONE RIA (DSL # 4200) by Diagnostic Systems Laboratories, Inc. — Product Code CIZ

K854673 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL ANDROSTENEDIONE RIA (DSL # 4200)". The FDA issued a decision of Substantially Equivalent on January 22, 1986. The device falls under product code CIZ (Radioimmunoassay, Androstenedione), a Class I device regulated under 21 CFR 862.1075. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 1986
Date Received
November 21, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Androstenedione
Device Class
Class I
Regulation Number
862.1075
Review Panel
CH
Submission Type