K827891Substantially Equivalent

Ultrasonic Pulsed Echo Imaging System Rt30

Name: K827891 Ultrasonic Pulsed Echo Imaging System Rt30
Creator: General Electric Co.
Published: 1982-09-29
License: https://open.fda.gov/license/

General Electric Co., Schenectady NY / Traditional, Substantially Equivalent

FDA source

K827891 is the FDA 510(k) clearance record for ULTRASONIC PULSED ECHO IMAGING SYSTEM RT30, cleared for General Electric Co. on 1982-09-29. FDA records list 256 510(k) clearances for General Electric Co., from 1976-08-26 to 2011-12-22. As of 2026-09-10, FDA records show no recalls naming K827891.

Clearance record

Decision date: 1982-09-29
Received: 1982-08-11 (49 days to decision)
Review panel: Unknown
Applicant: General Electric Co. 1 River Rd., Schenectady NY
Third party review: No