Skip to content

Mobile Standing Frame

by Metatech Corp. 510(k)

Active United States

510(k) K924314

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK924314 Date12 Feb 1993ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 6 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
IPL
Device Class
Class II
Regulation
21 CFR Part 890.3900
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

A mobile standing frame is a device designed to provide support and stability for individuals with mobility impairments, enabling them to assume and maintain a standing position. It is classified as a wheelchair, standup device under FDA product code IPL and regulation number 890.3900, falling within the Physical Medicine specialty.

The device was cleared through the FDA 510(k) process under K924314, with a traditional clearance decision of substantially equivalent, granted on February 12, 1993. It is manufactured by Metatech Corp. and is intended for use in clinical or therapeutic settings where standing support is required.

Other devices from Metatech Corp.

See all devices from Metatech Corp. →

Questions

AI-generated answers, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the MOBILE STANDING FRAME used for?

    The MOBILE STANDING FRAME is designed to provide support and stability for individuals with mobility impairments, enabling them to assume and maintain a standing position in clinical or therapeutic settings where standing support is required.

  • How was the MOBILE STANDING FRAME cleared for market?

    The device was cleared through the FDA 510(k) process under K924314, with a traditional clearance decision of substantially equivalent, granted on February 12, 1993, based on its substantial equivalence to a predicate device.

  • Who manufactures the MOBILE STANDING FRAME and where is it located?

    The MOBILE STANDING FRAME is manufactured by Metatech Corp., located at P.O. Box 2050, Westminster, MD 21158, United States, as indicated in the device's authorization and registration details.