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Patient Trolley 540

by Merivaara Instrumentarium Corp.

510(k) K943529

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK943529 Date4 Oct 1994ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
FPO
Device Class
Class II
Regulation
21 CFR Part 880.6910
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 23 Sep 2026

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

The Patient Trolley 540 is a wheeled stretcher designed for general hospital use. It is a Class II medical device that provides a mobile platform for patient transport within healthcare facilities.

The device is supplied by Merivaara Instrumentarium Corp. and has received FDA 510(k) clearance with the K number K943529. It is not specified as single-use or reusable, and no information regarding sterility, MRI safety, or storage conditions is provided in the data.

Other devices from Merivaara Instrumentarium Corp.