Class Class II
AccuContour (K221706)
Description
AccuContour by Manteia Technologies Co., Ltd., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK221706
Clearance Date2023-03-09
Clearance TypeTraditional
Product CodeQKB
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K221706
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. AccuContour (K221706) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K191928 | AccuContour | Xiamen Manteia Technology , Ltd. | 2020 |
| K182624 | MIM - MRT Dosimetry | Mim Software, Inc. | 2018 |
| K181572 | Workflow Box | Mirada Medical, Ltd. | 2018 |
| K173636 | Velocity | Varian Medical Systems, Inc. | 2018 |
Trace the full predicate network for K221706
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.