Outpatient Products Co.
Country not established
- Devices
- 1
What Outpatient Products Co. makes
Outpatient Products Co. manufactures surgical drapes designed for use in general and plastic surgery procedures. These products are intended to maintain sterile field conditions during surgical interventions.
The company’s surgical drapes are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Drapes(Surgical, General & Plastic Surgery) Ref K852280
510(k) 510(k)
Frequently asked questions
How many devices does Outpatient Products Co. have in the registry?
The registry currently lists 1 device for Outpatient Products Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Outpatient Products Co.'s devices?
Among its 1 most recently registered device, Outpatient Products Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Outpatient Products Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Outpatient Products Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Outpatient Products Co. in the registry?
The most recently registered devices listed for Outpatient Products Co. include DRAPES(SURGICAL, GENERAL & PLASTIC SURGERY).