Marco Mfg.
Country not established
- Devices
- 1
What Marco Mfg. makes
Marco Mfg. produces disposable surgical drapes designed for single-use in operating room procedures to maintain sterile field conditions during surgery.
Their product portfolio is regulated as Class II devices under FDA 510(k) clearance requirements and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Drapes, Disposable Surgical Ref K782051
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marco Mfg. have in the registry?
The registry currently lists 1 device for Marco Mfg.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marco Mfg.'s devices?
Among its 1 most recently registered device, Marco Mfg. has devices listed in FDA 510(k) (1 device).
What risk classes do Marco Mfg.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Marco Mfg.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marco Mfg. in the registry?
The most recently registered devices listed for Marco Mfg. include DRAPES, DISPOSABLE SURGICAL.