510(k) K162702 ยท HST Apparatus, Traction, Non-Powered
Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table
| Applicant | Stl International, Inc., Puyallup WA, US |
| Decision | Substantially Equivalent, Dec 30, 2016 |
| Received | Sep 28, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162702
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.