Medical Device Manufacturer · US , Walker , MI

Sentry Medical Products, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1983

Total

Cleared

Denied

Sentry Medical Products, Inc. has 13 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 13 cleared submissions from 1983 to 1996. Primary specialty: Cardiovascular.

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

Sentry Medical Products, 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 - Sentry Medical Products, Inc.

13 devices

1-12 of 13

Cleared Jul 24, 1996

SENTRY RADIOTRANSLUCENT ECG ELECTRODES

K962122 · DRX

Cardiovascular · 54d

Cleared Mar 27, 1996

SENTRY DISPOSABLE DISPERSIVE ELECTRODE

K955636 · JOS

General & Plastic Surgery · 107d

Cleared Nov 02, 1994

SENTRY INSERTION TRAY

K942827 · FOS

General Hospital · 141d

Cleared Aug 30, 1994

SENTRY AQUEOUS GEL ECG ELECTRODES

K934000 · DRX

Cardiovascular · 378d

Cleared Feb 15, 1994

BABY BOARD

K935098 · BTX

General & Plastic Surgery · 113d

Cleared Jan 18, 1994

LEADWIRE

K933603 · DSA

Cardiovascular · 175d

Cleared Dec 27, 1993

PATIENT CABLE

K932704 · DSA

Cardiovascular · 207d

Cleared Nov 22, 1988

ACCUTEMP PLUS

K881670 · FMT

General Hospital · 218d

DIAGNOSTIC ECG DISPOSABLE ELECTRODE

K851522 · DRX

Cardiovascular · 192d

INFANT LIMB ELECTRODE

K844632 · DRX

Cardiovascular · 48d

Sentry Medical Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sentry Medical Products, Inc.

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