620 Fluoroscopic Table, Tilt or Power Medical Tab

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

510(k) Number

K905265 ↗

FDA Product Code

IXR

Device Class

Class II

Regulation

21 CFR Part 892.1980

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Fluoroscopic Table, Tilt or Power Tilting Med. Tab

  Not classified

  FDA 510(k) K904722 Active Cleared 23 Jan 1991

• Treatment Table Modification

  Class I

  FDA 510(k) K936303 Active Cleared 18 Mar 1994

• R1436, R1697, R1699, R1564, R1216, R1214, R854 & R1213

  Class I

  FDA 510(k) K861350 Active Cleared 2 May 1986

• Autorange Model 205

  Class I

  FDA 510(k) K822031 Active Cleared 26 Jul 1982

• Models 841, 842, 843, 851, 852 & 853 Elevating Tractio

  Class I

  FDA 510(k) K844712 Active Cleared 5 Mar 1985

• R1124 & R1686 Paraffin

  Class II

  FDA 510(k) K861344 Active Cleared 27 May 1986

See all devices from Tri W-G, Inc. →

• What is the primary purpose of the 620 Fluoroscopic Table?

  The 620 Fluoroscopic Table is designed to support patients during medical radiologic procedures. It provides a stable platform for imaging and features electrically powered components to assist clinicians in positioning the patient as needed.

• Does the table offer adjustable positioning features?

  Yes, the device is designed with electrically powered components that allow for positioning adjustments. Depending on the specific configuration, the table may be fixed or capable of tilting to accommodate various radiologic requirements.

• What is the regulatory status of this device?

  The 620 Fluoroscopic Table has received FDA 510(k) clearance under K905265. It is classified as a Class II medical device under regulation number 892.1980 and is identified by product code IXR.