Astroid Planning App
510(k) K173940
Astroid Planning App is a Class II device made by .Decimal, LLC, cleared under FDA 510(k) K173940 on 15 May 2018, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK173940 | Date15 May 2018 | StatusActive |
Official records
- FDA 510(k) database K173940
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MUJ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.5050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K173940
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| .decimal Astroid Planning App 3.x | 3.x | 00851147007120 | — | On the market |
Similar devices
Other devices filed under FDA product code MUJ (System, Planning, Radiation Therapy Treatment).
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- CORVUS RADIATION THERAPY PLANNING SYSTEM by Best Nomos
- Pinnacle Radiation Therapy Planning System by Philips Medical Systems (Cleveland), Inc.
- RayStation by RaySearch Laboratories AB (PUBL)
- Focus Radiation Treatment Planning System by Computerized Medical Systems, Inc.
- syngo.via RT Image Suite by SIEMENS MEDICAL SOLUTIONS USA, INC.