510(k) K955376

IMMULITE HGH by Diagnostic Products Corp. — Product Code CFL

K955376 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE HGH". The FDA issued a decision of Substantially Equivalent on February 16, 1996. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

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