Arvey Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Arvey Corp. makes
Arvey Corp. manufactures steam sterilization indicators, including the MEDI + BIO SAFE STEAM STERILIZATION INDICATOR, which verifies the effectiveness of sterilization cycles in medical facilities. They also produce the MASTER-CHEK BOWIE-DICK TYPE TEST kit, used for validating the performance of autoclaves and other sterilization equipment.
The company’s products fall under FDA Class II medical devices and are listed via the 510(k) pathway. These devices are regulated under US jurisdiction and are intended for compliance with sterilization validation standards in healthcare settings.
Catalogue
Medi + Bio Safe Steam Steriliz. Indicat Ref K821997
Regimes: 510(k) Registry: 510(k)Master-Chek Bowie-Dick Type Test Ref K843182
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arvey Corp. have in the registry?
The registry currently lists 2 devices for Arvey Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arvey Corp.'s devices?
Among its 2 most recently registered devices, Arvey Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arvey Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arvey Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arvey Corp. in the registry?
The most recently registered devices listed for Arvey Corp. include MEDI + BIO SAFE STEAM STERILIZ. INDICAT and MASTER-CHEK BOWIE-DICK TYPE TEST.