510(k) K170578 ยท LRK Device, Anti-Snoring
True Function Adjustable Herbst Appliances
| Applicant | True Function Laboratory, Inc., La Mesa CA, US |
| Decision | Substantially Equivalent, Nov 24, 2017 |
| Received | Feb 27, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K170578
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.