Delaware Industries, Inc.
Country not established
- Devices
- 1
What Delaware Industries, Inc. makes
Delaware Industries, Inc. manufactures latex patient examination gloves designed for medical use, providing barrier protection during clinical procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891509
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Delaware Industries, Inc. have in the registry?
The registry currently lists 1 device for Delaware Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Delaware Industries, Inc.'s devices?
Among its 1 most recently registered device, Delaware Industries, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Delaware Industries, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Delaware Industries, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Delaware Industries, Inc. in the registry?
The most recently registered devices listed for Delaware Industries, Inc. include PATIENT EXAMINATION GLOVES (LATEX).