Arvik Enterprises/ Mini Lap Technologies
Country not established
- Devices
- 1
What Arvik Enterprises/ Mini Lap Technologies makes
Arvik Enterprises/Mini Lap Technologies manufactures the Arvik Laparoscopic Aspiration Instrument, a device designed for surgical aspiration during minimally invasive procedures, including laparoscopic surgery.
The company’s portfolio is regulated under Class I medical devices in the U.S. and listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Arvik Laparoscopic Aspiration Instrument Ref K102274
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arvik Enterprises/ Mini Lap Technologies have in the registry?
The registry currently lists 1 device for Arvik Enterprises/ Mini Lap Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arvik Enterprises/ Mini Lap Technologies's devices?
Among its 1 most recently registered device, Arvik Enterprises/ Mini Lap Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Arvik Enterprises/ Mini Lap Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arvik Enterprises/ Mini Lap Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arvik Enterprises/ Mini Lap Technologies in the registry?
The most recently registered devices listed for Arvik Enterprises/ Mini Lap Technologies include ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT.