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Plurix B Radiographic Table

by Tecnomed, Inc. 510(k)

Active United States

510(k) K781067

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK781067 Date17 Jul 1978ClearedStatusActive

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  • Withdrawn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
IXQ
Models / Variants
Device Class
Class II
Regulation
21 CFR Part 892.1980
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 21 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 Plurix B is a stationary top radiographic table designed for use in radiology settings. It functions as a support surface for patients during radiographic procedures.

This device is classified as a Class II medical device under regulation number 892.1980. It has received FDA 510(k) clearance, identified by submission number K781067.

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