Quadra Logic Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Quadra Logic Technologies, Inc. makes
Quadra Logic Technologies, Inc. manufactures the QLT ABSOLUTE URINE-HCG PREGNANCY TEST, a diagnostic device designed to detect human chorionic gonadotropin (hCG) in urine samples for pregnancy confirmation.
This product is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Qlt Absolute Urine-Hcg Pregnancy Test Ref K881806
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Quadra Logic Technologies, Inc. have in the registry?
The registry currently lists 1 device for Quadra Logic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quadra Logic Technologies, Inc.'s devices?
Among its 1 most recently registered device, Quadra Logic Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Quadra Logic Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Quadra Logic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quadra Logic Technologies, Inc. in the registry?
The most recently registered devices listed for Quadra Logic Technologies, Inc. include QLT ABSOLUTE URINE-HCG PREGNANCY TEST.