The following data is part of a premarket notification filed by Medix Biotech, Inc. with the FDA for Medix Visual Urine Hcg (7/7) Test.
Device ID | K850949 |
510k Number | K850949 |
Device Name: | MEDIX VISUAL URINE HCG (7/7) TEST |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | MEDIX BIOTECH, INC. 1420 STAFFORD ST. Redwood City, CA 94063 |
Contact | Shaw J Bian |
Correspondent | Shaw J Bian MEDIX BIOTECH, INC. 1420 STAFFORD ST. Redwood City, CA 94063 |
Product Code | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-03-07 |
Decision Date | 1985-04-12 |