510(k) K243813 ยท PCH Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System
QIAstat-Dx GI Panel 2 Mini B&V
| Applicant | QIAGEN GmbH, Hilden, DE |
| Decision | Substantially Equivalent, Jan 8, 2025 |
| Received | Dec 11, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243813
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.