Medical Device Manufacturer · US , Mchenry , IL

Sporicidin Intl. - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 1983

8

Total

7

Cleared

0

Denied

Sporicidin Intl. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1983 to 2000. Primary specialty: General Hospital.

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

Sporicidin Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sporicidin Intl.

8 devices

1-8 of 8

Cleared Nov 07, 2000

MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION

General Hospital · 41d

Cleared Mar 05, 1999

SPORICIDIN STERILIZING AND DISINFECTING SOLUTION (SSDS)

General Hospital · 175d

Cleared Feb 12, 1993

SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI

General Hospital · 80d

Cleared Sep 15, 1992

SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT

General Hospital · 126d

Cleared May 18, 1992

SPORICIDIN BRAND DISINFECTANT TOWELETTES

General Hospital · 587d

Cleared May 18, 1992

SPORICIDIN BRAND DISINFECTANT SPRAY

General Hospital · 587d

Cleared May 18, 1992

SPORICIDIN BRAND DISINFECTANT SOLUTION

General Hospital · 587d

Cleared Jun 30, 1983

SPORIDIDIN-D COLD STERILIZING/SOLUTION

Gastroenterology & Urology · 114d