Medical Device Manufacturer · US , Mchenry , IL

Quinton, Inc. - FDA 510(k) Cleared Devices

164 submissions · 160 cleared · Since 1976

164

Total

160

Cleared

0

Denied

FDA 510(k) Regulatory Record - Quinton, Inc. Gastroenterology & Urology ✕

51 devices

1-12 of 51

Cleared Sep 13, 1996

MAHURKAR 8 FR DUAL LEMEN CATHETER

Gastroenterology & Urology · 317d

Cleared May 09, 1990

MODIFIED PERM-CATH

Gastroenterology & Urology · 76d

Cleared Jan 29, 1990

MODIFIED QUINTON SINGLE LUMEN CATHETER

Gastroenterology & Urology · 91d

Cleared Jun 08, 1989

QUINTON SINGLE LUMEN CATHETER

Gastroenterology & Urology · 34d

Cleared Mar 27, 1989

PERITONEAL CATHETERS WITH AN ADDED FUNCTION

Gastroenterology & Urology · 67d

Cleared Feb 22, 1988

MODIFIED FORMED-EXTENSION MAHURKAR DUAL LUMEN CATH

Gastroenterology & Urology · 13d

Cleared Feb 17, 1988

PERMCATH INSERTION TRAY

Gastroenterology & Urology · 100d

Cleared Dec 29, 1987

BENT NECK CURLCATH PERITONEAL DIALYSIS KIT

Gastroenterology & Urology · 50d

Cleared Dec 09, 1987

PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)

Gastroenterology & Urology · 26d

Cleared Jun 17, 1987

ADULT PERM-CATH 40CM.

Gastroenterology & Urology · 43d

Cleared Jun 17, 1987

PERM-CATH CATHETER KIT

Gastroenterology & Urology · 29d

Cleared May 18, 1987

MODIFIED USE OF PULL-APART INTRODUCER SET

Gastroenterology & Urology · 13d

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