Lazarus Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Lazarus Medical, Inc. makes
Lazarus Medical, Inc. manufactures cannula introduction sets, which are used for guiding catheters or other medical instruments into blood vessels or other anatomical structures during procedures.
These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Cannula Introduction Set Ref K910015
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lazarus Medical, Inc. have in the registry?
The registry currently lists 2 devices for Lazarus Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lazarus Medical, Inc.'s devices?
Among its 2 most recently registered devices, Lazarus Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lazarus Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lazarus Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lazarus Medical, Inc. in the registry?
The most recently registered devices listed for Lazarus Medical, Inc. include PHONERIS INNER CANNULAE WITH PHONERIS AERO-FLEX VENTILATOR CIRCUIT CONNECTOR and CANNULA INTRODUCTION SET.