L.O.N. Research, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
Catalogue
Disposable Transducer Manifold Ref K890676
510(k) 510(k)L.O.N. Reusable Manifolds & Stopcocks Ref K812407
510(k) 510(k)Angioplasty Balloon Inflation Device Ref K880158
510(k) 510(k)L.O.N. Pres Mon Lines, Cpc Lines, Administration Ref K853099
510(k) 510(k)L.O.N. Disposable Coronary Manifold Ref K812408
510(k) 510(k)
Frequently asked questions
How many devices does L.O.N. Research, Inc. have in the registry?
The registry currently lists 5 devices for L.O.N. Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L.O.N. Research, Inc.'s devices?
Among its 5 most recently registered devices, L.O.N. Research, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do L.O.N. Research, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for L.O.N. Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from L.O.N. Research, Inc. in the registry?
The most recently registered devices listed for L.O.N. Research, Inc. include DISPOSABLE TRANSDUCER MANIFOLD, L.O.N. REUSABLE MANIFOLDS & STOPCOCKS, ANGIOPLASTY BALLOON INFLATION DEVICE and L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION.