K760559Substantially Equivalent

Patient Monitoring System

Name: K760559 Patient Monitoring System
Creator: General Electric Co.
Published: 1976-09-10
License: https://open.fda.gov/license/

General Electric Co., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K760559 is the FDA 510(k) clearance record for PATIENT MONITORING SYSTEM, cleared for General Electric Co. on 1976-09-10. 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 K760559.

Clearance record

Decision date: 1976-09-10
Received: 1976-09-02 (8 days to decision)
Review panel: Unknown
Applicant: General Electric Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No