Posey Sitter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K920206 ↗

FDA Product Code

KMI

Device Class

Class I

Regulation

21 CFR Part 880.2400

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Posey Bed

  Class I

  FDA 510(k) K113355 Active Cleared 2 May 2012

• Pediatric Limb Holders

  Class I

  FDA 510(k) K963439 Active Cleared 19 Nov 1996

• Posey Straight Jackets

  Class I

  FDA 510(k) K963410 Active Cleared 22 Nov 1996

• Jackets and Vests

  Class I

  FDA 510(k) K963442 Active Cleared 22 Nov 1996

• Restraint Accessories

  Class I

  FDA 510(k) K963436 Active Cleared 22 Nov 1996

• Pelvic Holders

  Class I

  FDA 510(k) K963437 Active Cleared 19 Nov 1996

See all devices from J. T. Posey Co. →