510(k) K950510

OCTEIA IGF-1 KIT by Immunodiagnostic Systems , Ltd. — Product Code CFL

K950510 is an FDA 510(k) premarket notification submitted by Immunodiagnostic Systems , Ltd. for the device "OCTEIA IGF-1 KIT". The FDA issued a decision of Substantially Equivalent on April 5, 1995. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Immunodiagnostic Systems , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 1995
Date Received
February 6, 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