United Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
United Biotech, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
United Biotech, Inc. has 22 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 22 cleared submissions from 1985 to 1998. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by United Biotech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - United Biotech, Inc.
22 devices
Cleared
Sep 15, 1998
UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVE
Chemistry
134d
Cleared
Jul 22, 1998
UBI MAGIWEL MARIJUANA METABOLITES
Toxicology
334d
Cleared
Feb 09, 1998
UBI MAGIWEL C-REACTIVE PROTEIN(CRP) QUANTITATIVE
Immunology
136d
Cleared
Oct 28, 1997
UBI MAGIWEL AMPHETAMINE METABOLITES
Toxicology
67d
Cleared
Oct 28, 1997
UBI MAGIWEL OPIATE METABOLITES
Toxicology
67d
Cleared
Oct 28, 1997
UBI MAGIWEL COCAINE METABOLITES
Toxicology
67d
Cleared
Jul 08, 1996
UBI MAGIWEL THYROXINE (T4) QUANTITATIVE
Chemistry
28d
Cleared
May 30, 1996
UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE
Chemistry
62d
Cleared
Jul 05, 1995
UBI MAGIWEL FERRITIN QUANTITATIVE
Immunology
68d
Cleared
Aug 10, 1993
UBI MAGIWEL(TM) HELICOBACTER PYLORI IGG
Microbiology
327d
Cleared
Jan 31, 1991
UBI MAGIWEL CORTISOL QUANTITATIVE
Chemistry
56d
Cleared
Jan 25, 1991
UBI MAGIWEL(TM) ANA QUANTITATIVE
Immunology
21d