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X-Ray Diagnostic Table YSF-200-30-90

by Shimadzu Medical Systems

510(k) K920722

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 NumberK920722 Date13 Apr 1992ClearedStatusActive

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  • Withdrawn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
IXR
Device Class
Class II
Regulation
21 CFR Part 892.1980
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 1 Oct 2026

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

The X-Ray Diagnostic Table YSF-200-30-90 is a radiographic, tilting table designed for use in radiology procedures. It is classified as a Class II medical device and serves as a platform for positioning patients during X-ray imaging, enabling adjustable angles and precise alignment for diagnostic imaging.

This table is supplied as a reusable medical device intended for use in radiology departments. It is cleared under FDA 510(k) with the K-number K920722, granted in 1992, and falls under the product code IXR. The device is not specified as single-use or sterile, and its MRI safety status is not indicated in the available data. Storage and maintenance instructions are not provided in the regulatory records.

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