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Patlog, Patlog Patient Handling System, Patlog Toplog Table Top, Model(S) 1.0, 1.0, C

by Oncolog Medical QA AB

510(k) K090044

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 NumberK090044 Date22 Jan 2009ClearedStatusActive

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  • Withdrawn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
IYE
Device Class
Class II
Regulation
21 CFR Part 892.5050
Advisory Committee
Radiology
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.

The Patlog Patient Handling System, including the Patlog Toplog Table Top, is a medical device designed for patient positioning in radiology applications. It functions as an accessory for a linear medical accelerator to facilitate the handling and support of patients during procedures.

This device is classified as a Class II medical device and has received FDA 510(k) clearance under K090044. It is available in models 1.0 and C, and is manufactured by Oncolog Medical QA AB.

Other devices from Oncolog Medical QA AB

  • Patlog 2.0

    Class II

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 primary purpose of the Patlog Patient Handling System?

    The Patlog system is designed to facilitate the positioning and support of patients during radiology applications. It serves as an accessory for a linear medical accelerator to ensure stable patient placement throughout the procedure.

  • Which models are available for this device?

    The Patlog Patient Handling System is available in model 1.0 and model C. Both models are part of the system designed for use with linear medical accelerators.

  • What is the regulatory classification of this device?

    The Patlog Patient Handling System is classified as a Class II medical device. It has received FDA 510(k) clearance under the number K090044.