S&W Model High-Low Mat Table, Various Models

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K864817 ↗

FDA Product Code

INQ

Device Class

Class I

Regulation

21 CFR Part 890.3760

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• S & W Model Aso

  Class II

  FDA 510(k) K830873 Active Cleared 13 May 1983

• S & W SW52E W/Power Back Lift

  Class I

  FDA 510(k) K832768 Active Cleared 20 Sep 1983

• S & W Model 29

  Class II

  FDA 510(k) K830875 Active Cleared 8 Apr 1983

• Tilt Table 53

  Class I

  FDA 510(k) K841145 Active Cleared 13 Apr 1984

• S & W Model Sw 37

  Class I

  FDA 510(k) K830874 Active Cleared 8 Apr 1983