Medical Device Manufacturer · US , Plymouth , MN

Interrad Medical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008

Recent clearances: SecurAcath, SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F, SecurAcath

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interrad Medical, Inc. General Hospital ✕

6 devices

1-6 of 6

Cleared Apr 12, 2021

General Hospital · 41d

Cleared Jun 26, 2018

General Hospital · 95d

Cleared Apr 27, 2012

General Hospital · 30d

Cleared Jul 09, 2010

SECURACATH UNIVERSAL

General Hospital · 345d

Cleared Mar 04, 2009

MODIFICATION TO SECURACATH, MODEL: SPK01

General Hospital · 139d

Cleared Sep 30, 2008

SECURACATH CATHETER, MODEL SPK01

General Hospital · 74d