Medical Device Manufacturer · US , Mchenry , IL

Oxford Medilog, Inc. - FDA 510(k) Cleared Devices

48 submissions · 48 cleared · Since 1978

Total

Cleared

Denied

Oxford Medilog, Inc. has 48 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 48 cleared submissions from 1978 to 1994. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Oxford Medilog, Inc.

48 devices

1-12 of 48

Cleared Jan 05, 1994

MODEL MEDILOG RAPIDE

K923737 · BZQ

Anesthesiology · 527d

Cleared Aug 18, 1992

MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)

K920295 · DQK

Cardiovascular · 209d

Cleared Jan 09, 1992

MODEL SONICAID AXIS

K912890 · HGM

Obstetrics & Gynecology · 192d

Cleared Dec 31, 1991

SONICAID TEAM

K912639 · HGM

Obstetrics & Gynecology · 200d

SONICAID MODEL MERIDIAN 800

K902690 · HGM

Obstetrics & Gynecology · 231d

Cleared Jul 09, 1990

SONICAID MODEL VASOFLO 4

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM

K891383 · OLZ

Neurology · 84d

Cleared Apr 20, 1989

MEDILOG 6000-FD REPORT GENERATOR

MEDILOG 9000-II AMBULATORY RECORDER

K890647 · DSH

Cardiovascular · 33d

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Oxford Medilog, Inc. - FDA 510(k) Cleared Devices

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