Frigitronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Frigitronics, Inc. makes
Frigitronics, Inc. manufactures hysteroscopic insufflators, including the Hysteromat Hysteroflator, as well as hysteroscopes and accessories in the HT4-series. The company also produces medical camera and light source systems under the HC-series, designed for gynecological procedures.
These devices are regulated under FDA 510(k) clearance, with classifications spanning Class I and Class II. The portfolio is listed in the FDA’s 510(k) database, and the company is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
HT4-Series Hysteroscopes And Accessories Ref K905392
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Frigitronics, Inc. have in the registry?
The registry currently lists 3 devices for Frigitronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Frigitronics, Inc.'s devices?
Among its 3 most recently registered devices, Frigitronics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Frigitronics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Frigitronics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Frigitronics, Inc. in the registry?
The most recently registered devices listed for Frigitronics, Inc. include HYSTEROMAT HYSTEROFLATOR HYSTEROSCOPIC INSUFFLATOR, HT4-SERIES HYSTEROSCOPES AND ACCESSORIES and HC-SERIES MEDICAL CAMERA/LIGHT SOURCE AND ACCESSOR.