Medical Device Manufacturer · US , Mchenry , IL

Survival Technology, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1977

Total

Cleared

Denied

Survival Technology, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1977 to 1993.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Survival Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Survival Technology, Inc.

10 devices

1-10 of 10

Cleared Jan 28, 1993

CARDIOBEEPER(R) CB-IIA

K925535 · DXH

Cardiovascular · 87d

Cleared Oct 03, 1989

CARDIOBEEPER MEMORY MONITOR CB 600 SERIES

General Hospital · 22d

Cleared May 12, 1988

CARDIOBEEPER(R) III

K880300 · DXH

Cardiovascular · 108d

Cleared Feb 08, 1985

CARDIOBEEPER PROFILE MONITOR

CARDIOBEEPER MEMORY MONITOR

K813101 · DXY

Cardiovascular · 24d

Cleared Dec 08, 1977

PACER MONITOR, PULSE WIDTH

K772178 · DXH

Cardiovascular · 16d

Survival Technology, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Survival Technology, Inc.

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