W.E. Leder Enterprises, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What W.E. Leder Enterprises, Inc. makes
W.E. Leder Enterprises, Inc. manufactures laryngoscopes, anesthesia apparatus (including models D-25, FO 20S, and PH-35), and a cardio-scope mini monitor for cardiac monitoring. Their portfolio also includes the ARF 850 E, a device used in anesthesia systems.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. Their anesthesia apparatus and monitoring devices are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Laryngescope Ref K831981
510(k) 510(k)Anesthesia Apatatus #d-25 Ref K830161
510(k) 510(k)Cardio-Scope Mini Monitor Ref K831878
510(k) 510(k)Arf 850 E Ref K831877
510(k) 510(k)Anesthesia Apparatus #fo 20S Ref K830160
510(k) 510(k)Anesthesia Apparatus Ph-35 Ref K830159
510(k) 510(k)
Frequently asked questions
How many devices does W.E. Leder Enterprises, Inc. have in the registry?
The registry currently lists 6 devices for W.E. Leder Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list W.E. Leder Enterprises, Inc.'s devices?
Among its 6 most recently registered devices, W.E. Leder Enterprises, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do W.E. Leder Enterprises, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for W.E. Leder Enterprises, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from W.E. Leder Enterprises, Inc. in the registry?
The most recently registered devices listed for W.E. Leder Enterprises, Inc. include LARYNGESCOPE, ANESTHESIA APATATUS #D-25, CARDIO-SCOPE MINI MONITOR and ARF 850 E.