Medical Device Manufacturer · US , Mchenry , IL

Ethox Corp. - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1977

Recent clearances: ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS, CUF-COVER (TM), TUM-E-VAC

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.

510(k) submissions have been managed by Entela, Inc. as regulatory consultant.

Ethox Corp. is one of 13090 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - 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) Regulatory Record - Ethox Corp.

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