E Med Future
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Needle Zap Ref P010065
PMA PMA
FDA recalls
2002
- 15 Aug 2002 Z-0624-03 Unclassified (pre-2012) Terminated Their NeedleZap devices were not manufactured in accordance with the Quality System Regulations, and were shipped without an approved PMA.
Full distribution text
- 15 Aug 2002 Z-0624-03 Unclassified (pre-2012) Terminated Their NeedleZap devices were not manufactured in accordance with the Quality System Regulations, and were shipped without an approved PMA.
Frequently asked questions
How many devices does E Med Future have in the registry?
The registry currently lists 1 device for E Med Future. Devices recorded under merged duplicate company entries are counted once.
Which registries list E Med Future's devices?
Among its 1 most recently registered device, E Med Future has devices listed in FDA PMA (1 device).
What risk classes do E Med Future's devices fall under?
Among its 1 most recently registered device, the classes recorded for E Med Future's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for E Med Future?
FDA recall records list 1 recall initiated by E Med Future, the most recent initiated on 2002-08-15. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from E Med Future in the registry?
The most recently registered devices listed for E Med Future include NEEDLE ZAP.