Medical Device Manufacturer · US , Mchenry , IL

Medtel Pty. , Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1979

8

Total

8

Cleared

0

Denied

Medtel Pty. , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1979 to 1983. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medtel Pty. , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtel Pty. , Ltd.

8 devices

1-8 of 8

Cleared Oct 28, 1983

PORTABLE OPERAT. RM. MONITORS HS30/40

Anesthesiology · 102d

Cleared Apr 09, 1982

HS17/HS18 SERIES MONITORS

General Hospital · 29d

Cleared Apr 01, 1982

CM10 CENTRAL MONITORING SYSTEM

Cardiovascular · 21d

Cleared Mar 22, 1982

HS20 PORT. OPERATING ROOM MONITOR

Cardiovascular · 39d

Cleared Sep 26, 1980

HS10 PORTABLE OPERATING ROOM MONITOR

Cardiovascular · 16d

Cleared Apr 10, 1980

D668 & D664 CENTRAL MONITORING SYSTEMS

Cardiovascular · 65d

Cleared Oct 01, 1979

HSH/H512 ADULT PHYSIOLOGICAL MONITORS

Cardiovascular · 17d

Cleared Oct 01, 1979

H59 CRITICAL CARE MONITOR

Cardiovascular · 17d