The following data is part of a premarket notification filed by Hill Laboratories Co. with the FDA for The Hill Adjustable Podiatry Model.
| Device ID | K952357 |
| 510k Number | K952357 |
| Device Name: | THE HILL ADJUSTABLE PODIATRY MODEL |
| Classification | Table, Powered |
| Applicant | HILL LABORATORIES CO. 445 LINCOLN HIGHWAY Malvern, PA 19355 |
| Contact | Howard A Hill |
| Correspondent | Howard A Hill HILL LABORATORIES CO. 445 LINCOLN HIGHWAY Malvern, PA 19355 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-04-27 |
| Decision Date | 1995-07-06 |