Heatmax Mfg., Inc.
Country not established
- Devices
- 1
What Heatmax Mfg., Inc. makes
Heatmax Mfg., Inc. manufactures the MEDI-PACK, a Class I medical device designed for single-use thermal therapy applications in clinical settings.
The MEDI-PACK is regulated under the FDA’s 510(k) pathway and is listed as a Class I device. The company is based in the United States.
Catalogue
Medi-Pack Ref K895860
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heatmax Mfg., Inc. have in the registry?
The registry currently lists 1 device for Heatmax Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heatmax Mfg., Inc.'s devices?
Among its 1 most recently registered device, Heatmax Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Heatmax Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Heatmax Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Heatmax Mfg., Inc. in the registry?
The most recently registered devices listed for Heatmax Mfg., Inc. include MEDI-PACK.