510(k) K972061 · LRK Device, Anti-Snoring

TOA

Applicant	W. Keith Thornton, D.D.S., Dallas TX, US
Decision	Substantially Equivalent, Aug 21, 1997
Received	Jun 3, 1997
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K972061

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.