Precision Therapy Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Precision Therapy Intl., Inc. makes
Precision Therapy Intl., Inc. develops software tools for radiation therapy planning, including RENDER-PLAN 3-D 4.00, PRECISE-PLAN 1.0, and PRECISEPLAN 2.0, which support 3D treatment simulation and dose calculation. The company also manufactures the HERCULES RADIATION THERAPY COUCH, a specialized patient positioning device for radiation oncology.
These products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Render-Plan 3-D 4.00 & Precise-Plan 1.0 Ref K002240
Regimes: 510(k) Registry: 510(k)Render-Plan 3-D Ref K992864
Regimes: 510(k) Registry: 510(k)Preciseplan 2.0 Ref K022411
Regimes: 510(k) Registry: 510(k)Hercules Radiation Therapy Couch Ref K950061
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Therapy Intl., Inc. have in the registry?
The registry currently lists 4 devices for Precision Therapy Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Therapy Intl., Inc.'s devices?
Among its 4 most recently registered devices, Precision Therapy Intl., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Precision Therapy Intl., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Precision Therapy Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Therapy Intl., Inc. in the registry?
The most recently registered devices listed for Precision Therapy Intl., Inc. include RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0, RENDER-PLAN 3-D, PRECISEPLAN 2.0 and HERCULES RADIATION THERAPY COUCH.