510(k) K960551

DSL ACTIVE HUMAN GROWTH HORMONE ELISA by Diagnostic Systems Laboratories, Inc. — Product Code CFL

K960551 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL ACTIVE HUMAN GROWTH HORMONE ELISA". The FDA issued a decision of Substantially Equivalent on March 6, 1996. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 6, 1996
Date Received
February 8, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Human Growth Hormone
Device Class
Class I
Regulation Number
862.1370
Review Panel
CH
Submission Type