Safeway Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Safeway Products, Inc. makes
Safeway Products, Inc. makes soft lens thermal disinfecting units, patient examination gloves (latex), and Aqualux lens cases.
The company's devices are classified as Class I, Class II, and unclassified (U) and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Soft Lens Thermal Disinfecting Unit, A-C Ref K822828
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K891508
Regimes: 510(k) Registry: 510(k)Aqualux Lens Case Ref K862811
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Safeway Products, Inc. have in the registry?
The registry currently lists 3 devices for Safeway Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safeway Products, Inc.'s devices?
Among its 3 most recently registered devices, Safeway Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Safeway Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Safeway Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Safeway Products, Inc. in the registry?
The most recently registered devices listed for Safeway Products, Inc. include SOFT LENS THERMAL DISINFECTING UNIT, A-C, PATIENT EXAMINATION GLOVES (LATEX) and AQUALUX LENS CASE.