510(k) K952319

CONTRAST & RAPID HCG URINE/SERUM TST by Medix Biotech, Inc. — Product Code JHI

K952319 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "CONTRAST & RAPID HCG URINE/SERUM TST". The FDA issued a decision of Substantially Equivalent on June 20, 1995. 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
June 20, 1995
Date Received
May 18, 1995
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