Jack Speer and Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Jack Speer and Assoc., Inc. makes
Jack Speer and Assoc., Inc. manufactures reprocessed compression sleeve devices designed for medical use, including those intended for venous return support or limb circulation management.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Jsa Reprocessed Compression Sleeve Devices Ref K031722
Regimes: 510(k) Registry: 510(k)Jsa's Reprocessed Compression Sleeve Devices Ref K040065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jack Speer and Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Jack Speer and Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jack Speer and Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Jack Speer and Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Jack Speer and Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Jack Speer and Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jack Speer and Assoc., Inc. in the registry?
The most recently registered devices listed for Jack Speer and Assoc., Inc. include JSA REPROCESSED COMPRESSION SLEEVE DEVICES and JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES.