Emde Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Emde Corp. makes
Emde Corp. manufactures emergency communication devices, including the MARZ-175 for critical alerts and the QWIK-CALL for rapid response signaling. Their product line also includes the MOSQUITO, a portable blood sampling device, and the MOSQUITO ARTERIAL BLOOD SAMPLER, designed for arterial blood collection.
The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. These devices are listed in the FDA’s 510(k) clearance registry. Emde Corp. is based in the United States.
Catalogue
Marz-175 Ref K811199
Regimes: 510(k) Registry: 510(k)Qwik-Call Ref K860052
Regimes: 510(k) Registry: 510(k)Mosquito Ref K771013
Regimes: 510(k) Registry: 510(k)Mosquito Arterial Blood Sampler Ref K791465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emde Corp. have in the registry?
The registry currently lists 4 devices for Emde Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emde Corp.'s devices?
Among its 4 most recently registered devices, Emde Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Emde Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Emde Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emde Corp. in the registry?
The most recently registered devices listed for Emde Corp. include MARZ-175, QWIK-CALL, MOSQUITO and MOSQUITO ARTERIAL BLOOD SAMPLER.