Medical Device Manufacturer · US , Houston , TX

Hommed, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2000

8

Total

8

Cleared

0

Denied

Hommed, LLC has 8 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 8 cleared submissions from 2000 to 2004. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Hommed, LLC

8 devices

1-8 of 8

Cleared Aug 18, 2004

HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS

Cardiovascular · 142d

Cleared Aug 10, 2004

HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM

Cardiovascular · 152d

Cleared Feb 27, 2004

CENTRAL STATION, VERSION 3.3H

Cardiovascular · 50d

Cleared Apr 22, 2002

HOMMED CENTRAL STATION

Cardiovascular · 94d

Cleared Apr 09, 2002

HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER

Anesthesiology · 124d

Cleared Jun 28, 2001

HOMMED OBSERVER, MODEL I

Cardiovascular · 260d

Cleared Mar 02, 2001

HOMMED SENTRY III PATIENT MONITOR SYSTEM

Anesthesiology · 63d

Cleared Mar 15, 2000

THE HOMMED SENTRY, MODEL 1 SENTRY

Cardiovascular · 117d