Medical Device Manufacturer · US , Mchenry , IL

Gould, Inc. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1976

Total

Cleared

Denied

Gould, Inc. has 31 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 31 cleared submissions from 1976 to 1991.

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 - Gould, Inc.

31 devices

1-12 of 31

Cleared Jul 22, 1991

CARDIAC ELECTROPHYSICAL LEAD SELECTOR, MODIFIED

K911935 · DRR

Cardiovascular · 82d

Cleared Aug 18, 1986

MODEL SP1465 CARDIAC OUTPUT COMPUTER

K861092 · DXG

Cardiovascular · 147d

Cleared May 08, 1986

PRESSURE MONITOR CATH MODELS SP5325,SP5327,SP5337

K860805 · DQO

Cardiovascular · 65d

Cleared Feb 26, 1986

MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR

K855145 · DRS

Cardiovascular · 64d

Cleared Jan 14, 1986

MODEL 2120 SPIROSCREEN

K854403 · BZG

Anesthesiology · 75d

Cleared Oct 17, 1985

GOULD DISPOSABLE TRANSDUCER & ACCESSORIES-DTX

K851486 · DRS

Cardiovascular · 185d

Cleared Feb 22, 1985

C/PES 9201, ECG STRESS TESTING SYS

K850114 · DRT

Cardiovascular · 39d

Cleared Feb 08, 1985

C/PES 9103, ECG STRESS TESTING SYSTEM

K850113 · DRT

Cardiovascular · 25d

Cleared Feb 01, 1985

CARDIAC COMPUTER SP1445

K843555 · DXG

Cardiovascular · 144d

Cleared Jan 23, 1985

MODEL P23XL PHYSIOLOGICAL PRESSURE TRANSDUCER

K843969 · DXO

Cardiovascular · 104d

Cleared Oct 24, 1984

MODEL IM1074 END-TIDAL CO2 MODULE

K843970 · CCK

Anesthesiology · 13d

Cleared Jun 15, 1984

AUTOMATED NON-INVASIVE PRESSURE MODULE

K840909 · DXN

Cardiovascular · 107d

Gould, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gould, Inc.

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