510(k) K920299

MEDIX BIOTECH HGHENZYME IMMUNOASSAY TEST KIT by Medix Biotech, Inc. — Product Code CFL

K920299 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "MEDIX BIOTECH HGHENZYME IMMUNOASSAY TEST KIT". The FDA issued a decision of Substantially Equivalent on March 4, 1992. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 1992
Date Received
January 22, 1992
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