Digitcare Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Digitcare Corp. makes
Digitcare Corp. manufactures sterile intravenous (I.V.) starter kits for medical use, as well as seamless latex patient exam gloves designed for clinical examinations. The I.V. Start Kit is intended for initiating peripheral venous access, while the gloves provide barrier protection during patient assessments.
The company’s products are regulated under the FDA’s Class I and Class II categories, with relevant devices listed via the 510(k) pathway. These items are intended for domestic distribution within the United States.
Catalogue
Digitcare I.V. Start Kit Ref K905009
Regimes: 510(k) Registry: 510(k)Seamless Latex Patient Exam Gloves Ref K920700
Regimes: 510(k) Registry: 510(k)Seamless Latex Patient Examination Gloves Ref K891491
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digitcare Corp. have in the registry?
The registry currently lists 3 devices for Digitcare Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digitcare Corp.'s devices?
Among its 3 most recently registered devices, Digitcare Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Digitcare Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Digitcare Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digitcare Corp. in the registry?
The most recently registered devices listed for Digitcare Corp. include DIGITCARE I.V. START KIT, SEAMLESS LATEX PATIENT EXAM GLOVES and SEAMLESS LATEX PATIENT EXAMINATION GLOVES.