510(k) K961678

HUMAN GROWTH HORMONE IMMUNOASSAY KIT by Nichols Institute Diagnostics — Product Code CFL

K961678 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "HUMAN GROWTH HORMONE IMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on July 8, 1996. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 8, 1996
Date Received
May 1, 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