Medical Device Manufacturer · US , Mchenry , IL

Nova-Ventrx - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1981

Total

Cleared

Denied

Nova-Ventrx has 12 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1981 to 1997.

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

FDA 510(k) Regulatory Record - Nova-Ventrx

12 devices

1-12 of 12

Cleared Dec 02, 1997

CRITERION, CRITERION I.V., MODIFIED

K952267 · BZE

Anesthesiology · 932d

Cleared Dec 29, 1995

CONDENSATE COLLECTION KIT

K954480 · CAI

Anesthesiology · 94d

Cleared Aug 10, 1989

CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004

K893760 · BZO

Anesthesiology · 83d

Cleared Aug 15, 1988

RES-Q 1, 2, 3, 4 AND 5

K881207 · BTM

Anesthesiology · 147d

Cleared Mar 06, 1987

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011

K870382 · CBP

Anesthesiology · 36d

Cleared Nov 13, 1986

MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT

K863756 · BZO

Anesthesiology · 49d

Cleared May 02, 1985

CO-AX VENTILATOR CIRCUIT

K850600 · BZO

Anesthesiology · 76d

Cleared Oct 04, 1984

MAXI-MISER HUMIDIFIER INSERT 1020 & 1021

K842794 · BTT

Anesthesiology · 79d

Cleared Oct 04, 1984

MAXI-MISER HUMIDIFIER INSERT 1030

K842795 · BTT

Anesthesiology · 79d

Cleared May 30, 1984

MAXI-MISER HUMIDIFIER INSERT 1020

K841569

Cardiovascular · 43d

Cleared May 30, 1984

MAXI-MISER WATER TRANSFER SET 1021/1022

Nova-Ventrx - FDA 510(k) Cleared Devices

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