Laboratory Diagnostics Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Laboratory Diagnostics Co., Inc. makes
Laboratory Diagnostics Co., Inc. manufactures diagnostic test kits for laboratory use, including the QUICK CEPT for microbiological culture and the QUICK CULT SLIDE TEST for detecting fecal occult blood in stool samples.
These products are regulated as Class II medical devices in the US and are listed under the FDA’s 510(k) clearance process. The company operates from the United States.
Catalogue
Quick Cept Ref K801668
Regimes: 510(k) Registry: 510(k)Quick Cult Slide Test Fecal Occult Blood Ref K761232
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratory Diagnostics Co., Inc. have in the registry?
The registry currently lists 2 devices for Laboratory Diagnostics Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratory Diagnostics Co., Inc.'s devices?
Among its 2 most recently registered devices, Laboratory Diagnostics Co., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Laboratory Diagnostics Co., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Laboratory Diagnostics Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laboratory Diagnostics Co., Inc. in the registry?
The most recently registered devices listed for Laboratory Diagnostics Co., Inc. include QUICK CEPT and QUICK CULT SLIDE TEST FECAL OCCULT BLOOD.