Sascie
Country not established
- Devices
- 2
What Sascie makes
Sascie manufactures pregnancy testing devices, including the SAS SERUM/URINE HCG and SAS PREGNANCY STRIP, which are used to detect human chorionic gonadotropin (hCG) hormone in serum or urine samples.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry. Sascie is based in the US.
Catalogue
SAS Serum/Urine Hcg Ref K965250
Regimes: 510(k) Registry: 510(k)SAS Pregnancy Strip Ref K965253
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sascie have in the registry?
The registry currently lists 2 devices for Sascie. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sascie's devices?
Among its 2 most recently registered devices, Sascie has devices listed in FDA 510(k) (2 devices).
What risk classes do Sascie's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sascie's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sascie in the registry?
The most recently registered devices listed for Sascie include SAS SERUM/URINE HCG and SAS PREGNANCY STRIP.