Neal & Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Neal & Assoc., Inc. makes
Neal & Assoc., Inc. produces medical accessories for external pacemaker management, including sterile dressings for wire changes, and wrist cones designed for securing external leads during patient care.
Their portfolio includes Class I and Class II devices, all of which are listed via FDA 510(k) clearance. The company operates from the United States.
Catalogue
External Pacemaker Wire Dressing Change Ref K881356
Regimes: 510(k) Registry: 510(k)Neal Wrist Cones Ref K925924
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neal & Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Neal & Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neal & Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Neal & Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neal & Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neal & Assoc., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neal & Assoc., Inc. in the registry?
The most recently registered devices listed for Neal & Assoc., Inc. include EXTERNAL PACEMAKER WIRE DRESSING CHANGE and NEAL WRIST CONES.