510(k) K955376

IMMULITE HGH by Diagnostic Products Corp. — Product Code CFL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 1996
Date Received
November 24, 1995
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