Class Class II
Mould Probe MR Safe (K241764)
Description
Mould Probe MR Safe by Varian Medical Systems, Inc., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241764
Clearance Date2025-01-10
Clearance TypeTraditional
Product CodeJAQ
Regulation Number892.5700
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241764
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. Mould Probe MR Safe (K241764) cites 3 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162615 | Mould Applicator Set | Varian Medical Systems, Inc. | 2017 |
| K152018 | Varian Cleaning Caps, Varian Leak Stop Buttons, Varian Leak... | Varian Medical Systems, Inc. | 2015 |
| K073133 | INTERSTITIAL NEEDLES | Varian Medical Systems, Inc. | 2007 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241965 | Catheter Surface Flap Applicator Set (GM11011830) | Varian Medical Systems | 2024 |
Trace the full predicate network for K241764
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.