Image Transport Series III

by Dataview Imaging Intl., Inc. 510(k)

Active United States

510(k) K925964

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK925964	Date3 Feb 1995Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K925964
FDA Product Code: LMD

Device Class: Class I
Regulation: 21 CFR Part 892.2020
Advisory Committee: Radiology
FDA Decision: SESE Substantially Equivalent

Other devices from Dataview Imaging Intl., Inc.

Image Transport Series II

Class II