Qrp, Inc.
Country not established
- Devices
- 1
What Qrp, Inc. makes
Qrp, Inc. manufactures patient examination gloves, which are single-use barriers designed to protect healthcare providers during clinical examinations and procedures. These gloves are intended for general medical use, ensuring hygiene and reducing the risk of cross-contamination in patient care settings.
The company’s products fall under FDA Class I devices, which are subject to general controls and are typically exempt from premarket notification (510(k)) requirements unless they present a low-to-moderate risk. The patient examination gloves are listed with the FDA under the 510(k) pathway, indicating compliance with regulatory standards for medical device authorization. The company is based in the United States.
Catalogue
Patient Examination Glove Ref K942086
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Qrp, Inc. have in the registry?
The registry currently lists 1 device for Qrp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qrp, Inc.'s devices?
Among its 1 most recently registered device, Qrp, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Qrp, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Qrp, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Qrp, Inc. in the registry?
The most recently registered devices listed for Qrp, Inc. include PATIENT EXAMINATION GLOVE.