Medical Device Manufacturer · US , Walker , MI

North American Instrument Corp. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1983

Total

Cleared

Denied

North American Instrument Corp. has 28 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.

Historical record: 28 cleared submissions from 1983 to 1996.

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

FDA 510(k) Regulatory Record - North American Instrument Corp.

28 devices

1-12 of 28

Cleared Mar 29, 1996

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)

EPIC INTRODUCER SHEATH

K960310 · DYB

Cardiovascular · 16d

Cleared Mar 03, 1993

MORSE(R) ANGIOGRAPHIC CATHETERS

K922552 · DQO

Cardiovascular · 278d

Cleared Jun 10, 1992

MORSE HEMOSTATIC CATHETER INTRODUCER SET

K915078 · DYB

Cardiovascular · 215d

Cleared Jan 10, 1992

MORSE ANESTHESIA

K905208 · FPA

General Hospital · 416d

Cleared Sep 11, 1991

MORSE VASCULAR INTRODUCER SET

K912961 · DYB

Cardiovascular · 65d

Cleared Apr 22, 1991

THE PERCEPTOR(TM) STAND ALONE TRANSDUCER

K910764 · DRS

Cardiovascular · 81d

Cleared Mar 26, 1991

NAMIC CONTRAST SAVINGS DELIVERY SYSTEM

K903493 · IZI

Radiology · 235d

Cleared Jan 03, 1991

MORSE BALLOON INFLATION DEVICE

K904275 · MAV

Cardiovascular · 107d

Cleared Sep 27, 1990

GUIDEWIRE TORQUE DEVICE AND GUIDEWIRE INTRODUCER

North American Instrument Corp. - FDA 510(k) Cleared Devices

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