510(k) K952873

MEDIX BIOTECH STREP A ANTIGEN DETECTION TEST (MODIFICATION) by Medix Biotech, Inc. — Product Code GTZ

K952873 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "MEDIX BIOTECH STREP A ANTIGEN DETECTION TEST (MODIFICATION)". The FDA issued a decision of Substantially Equivalent on September 8, 1995. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 1995
Date Received
June 6, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, All Groups, Streptococcus Spp.
Device Class
Class I
Regulation Number
866.3740
Review Panel
MI
Submission Type