510(k) K022411 ยท MUJ System, Planning, Radiation Therapy Treatment
PRECISEPLAN 2.0
| Applicant | Precision Therapy Intl., Inc., Norcross GA, US |
| Decision | Substantially Equivalent, Sep 20, 2002 |
| Received | Jul 24, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022411
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 4, 2011 | Elekta, Inc. PrecisePLAN Treatment Planning System
Intended use: To plan multiple beam radiation therapy treatments. Terminated |
MUJ | None listed |
| Mar 2, 2011 | Elekta, Inc. PrecisePLAN Treatment Planning System
To plan multiple beam radiation therapy treatments. Terminated |
MUJ | None listed |
| Apr 16, 2010 | Elekta, Inc. PrecisePLAN 2.10 Treatment Planning System Terminated |
MUJ | None listed |
| Mar 16, 2010 | Elekta, Inc. PrecisePLAN 2.15 Treatment Planning System.
The product is used to plan multiple beam radiation therapy treatments. Terminated |
MUJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.