Pymah Corp., Ati Div.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Pymah Corp., Ati Div. makes
Pymah Corp., Ati Div. manufactures disposable biological test packs for sterilization validation, including steam sterilization and ethylene oxide processes. These packs are designed for use in monitoring biological indicators to ensure effective sterilization cycles in medical and healthcare settings.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States.
Catalogue
Ati-Pymah Disposable Biological Test Pack Ref K884767
510(k) 510(k)Ati-Pymah Disposable Steam Biological Test Pack Ref K884615
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Pymah Corp., Ati Div. have in the registry?
The registry currently lists 3 devices for Pymah Corp., Ati Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pymah Corp., Ati Div.'s devices?
Among its 3 most recently registered devices, Pymah Corp., Ati Div. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pymah Corp., Ati Div.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pymah Corp., Ati Div.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pymah Corp., Ati Div. in the registry?
The most recently registered devices listed for Pymah Corp., Ati Div. include ATI-PYMAH DISPOSABLE BIOLOGICAL TEST PACK, ATI-PYMAH DISPOSABLE STEAM BIOLOGICAL TEST PACK and ATI DISP. BIOLOGICAL TEST PACK FOR ETHYLENE OXIDE.