Medical Device Manufacturer · US , East Rutherford , NJ

Vital Signs, Inc. - FDA 510(k) Cleared Devices

75 submissions · 71 cleared · Since 1979

Total

Cleared

Denied

Vital Signs, Inc. has 71 FDA 510(k) cleared medical devices. Based in East Rutherford, US.

Historical record: 71 cleared submissions from 1979 to 2012. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Vital Signs, Inc.

75 devices

1-12 of 75

Cleared Mar 14, 2012

ENFLOW IV FLUID WARMER

K112902 · LGZ

General Hospital · 162d

BREAS PV 10I CPAP SYSTEM, MODEL PV 10I

K030985 · BZD

Anesthesiology · 201d

Cleared Aug 22, 2002

DISPOSABLE PRESSURE MANOMETER

General Hospital · 118d

Cleared Mar 07, 2001

BREAS HA50 HUMIDIFIER, MODEL HA50

K002454 · BTT

Anesthesiology · 209d

Cleared Aug 03, 2000

BREAS PV 100 CPAP SYSTEM

General Hospital · 61d

Cardiovascular · 203d

Cleared Jun 01, 1999

VITAL PEP

K984468 · BWF

Anesthesiology · 167d

Cleared Aug 21, 1997

T-WALL UNCUFFED TRACHEAL TUBE

K970196 · BTR

Anesthesiology · 212d

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Vital Signs, Inc. - FDA 510(k) Cleared Devices

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