Telemetry Monitor 5500 Release 4.0 (867232) (K242962)
Description
Telemetry Monitor 5500 Release 4.0 (867232) by Philips Medizin Systeme Böblingen GmbH, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242962
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. Telemetry Monitor 5500 Release 4.0 (867232) (K242962) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K180017 | MX40 Release C.01 | Philips Medical Systems | 2018 |
Trace the full predicate network for K242962
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.