510(k) K924259

MEDIX BIOTECH BESTEST(TM) HCG-URINE, CAT# B1H0100 by Medix Biotech, Inc. — Product Code JHI

K924259 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "MEDIX BIOTECH BESTEST(TM) HCG-URINE, CAT# B1H0100". The FDA issued a decision of Substantially Equivalent on November 25, 1992. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 25, 1992
Date Received
August 24, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Visual, Pregnancy Hcg, Prescription Use
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type