Partech Co., Inc.
Country not established
- Devices
- 1
What Partech Co., Inc. makes
Partech Co., Inc. manufactures latex patient examination gloves designed for clinical use, providing a barrier for medical professionals during examinations and procedures.
These gloves are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891340
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Partech Co., Inc. have in the registry?
The registry currently lists 1 device for Partech Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Partech Co., Inc.'s devices?
Among its 1 most recently registered device, Partech Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Partech Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Partech Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Partech Co., Inc. in the registry?
The most recently registered devices listed for Partech Co., Inc. include PATIENT EXAMINATION GLOVES (LATEX).