510(k) K241890 · MLO Electrocardiograph, Ambulatory, With Analysis Algorithm
Philips Holter Analysis System
| Applicant | Philips Medizin Systeme Böblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Mar 21, 2025 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241890
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.