Emily Iker M.D., A.P.C.
Country not established
- Devices
- 1
What Emily Iker M.D., A.P.C. makes
Emily Iker M.D., A.P.C. manufactures the DM Sleeve, a medical device designed for use in surgical procedures.
The DM Sleeve is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dm Sleeve Ref K021102
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emily Iker M.D., A.P.C. have in the registry?
The registry currently lists 1 device for Emily Iker M.D., A.P.C.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emily Iker M.D., A.P.C.'s devices?
Among its 1 most recently registered device, Emily Iker M.D., A.P.C. has devices listed in FDA 510(k) (1 device).
What risk classes do Emily Iker M.D., A.P.C.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Emily Iker M.D., A.P.C.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emily Iker M.D., A.P.C. in the registry?
The most recently registered devices listed for Emily Iker M.D., A.P.C. include DM SLEEVE.