FDA 510(k) Applications Submitted by Rylie Teeter Leier
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162702 | 09/28/2016 | Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table | STL International, Inc. |
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