Harbinger Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Harbinger Medical, Inc. makes
Harbinger Medical, Inc. manufactures the Micro-Induction 1000 System, a device designed for localized hyperthermia treatments, including modifications to existing systems. This system is intended for therapeutic applications involving controlled tissue heating.
The Micro-Induction 1000 System is classified as a Class II medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Modification To: Micro-Induction 1000 System Ref K090249
Regimes: 510(k) Registry: 510(k)Micro-Induction 1000 System Ref K013615
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Harbinger Medical, Inc. have in the registry?
The registry currently lists 2 devices for Harbinger Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harbinger Medical, Inc.'s devices?
Among its 2 most recently registered devices, Harbinger Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Harbinger Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Harbinger Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harbinger Medical, Inc. in the registry?
The most recently registered devices listed for Harbinger Medical, Inc. include MODIFICATION TO: MICRO-INDUCTION 1000 SYSTEM and MICRO-INDUCTION 1000 SYSTEM.