U.S. Drug Testing, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What U.S. Drug Testing, Inc. makes
U.S. Drug Testing, Inc. manufactures single-use assay columns and immunoassay systems for detecting and quantifying controlled substances in biological samples. Products include columns for opiates, cannabinoids (THC), amphetamines, PCP, cocaine and its metabolites, as well as a flow immunoassay system for laboratory testing.
The company’s portfolio comprises Class I and Class II devices, with some listed as Class U under FDA regulations. Devices are tracked via FDA’s 510(k) clearance process, and the manufacturer is based in the United States.
Catalogue
Usdt Opiate Assay Column Catalog No. 9000-200 Ref K932318
510(k) 510(k)Amphetamine Test System Ref K934693
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
Usdt Flow Immunoassay System, Model 9000 Ref K931227
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Drug Testing, Inc. have in the registry?
The registry currently lists 6 devices for U.S. Drug Testing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Drug Testing, Inc.'s devices?
Among its 6 most recently registered devices, U.S. Drug Testing, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do U.S. Drug Testing, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for U.S. Drug Testing, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Drug Testing, Inc. in the registry?
The most recently registered devices listed for U.S. Drug Testing, Inc. include USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200, AMPHETAMINE TEST SYSTEM, USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 and USDT PHENCYCLIDINE (PCP) ASSAY COLUMN CAT. NO. 9000-400.