Medical Device Manufacturer · US , Mchenry , IL

Ethox Corp. - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1977

Total

Cleared

Denied

Ethox Corp. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1977 to 2004. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Ethox Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Ethox Corp.

19 devices

1-12 of 19

Cleared Mar 15, 2004

ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS

Cardiovascular · 177d

Cleared Feb 21, 1997

TUM-E-VAC

K962850 · KDH

Gastroenterology & Urology · 214d

Cleared Sep 30, 1994

NO-MES

K935633 · KNT

Gastroenterology & Urology · 311d

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

K885220 · KNT

Gastroenterology & Urology · 279d

Cleared Sep 11, 1989

SURGI SQUEEZ

K894927 · KZD

General Hospital · 40d

Cleared Feb 10, 1989

SURGI-CUF STERILE/NON-STERILE DISPOSABLE

K883977 · DXQ

Cardiovascular · 143d

Cleared Mar 11, 1986

ETHOX LAVAGE TUBE

K860599 · KDH

Gastroenterology & Urology · 20d

Cleared Apr 04, 1985

ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.

K844988 · DXQ

Cardiovascular · 99d

Cleared May 21, 1984

ETHOX RELIA-FLO 2001 ENTERAL FEED

K841512 · FRN

General Hospital · 39d

Cleared May 01, 1984

WEIGHTED FEEDING TUBE W/PRE-INSERTED

K841014 · KNT

Gastroenterology & Urology · 53d

Ethox Corp. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Ethox Corp.

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