Interrad Medical, Inc.

Interrad Medical, Inc. holds 7 FDA 510(k) medical device clearances, first cleared 2008, most recent 2021.

Top product codes for Interrad Medical, Inc.

Recent clearances by Interrad Medical, Inc.

K210629 — SecurAcathCode OKC·2021-04-12
K180994 — SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FCode KMK·2019-07-09
K180769 — SecurAcathCode OKC·2018-06-26
K120935 — SECURACATHCode OKC·2012-04-27
K092306 — SECURACATH UNIVERSALCode LJS·2010-07-09
K083081 — MODIFICATION TO SECURACATH, MODEL: SPK01Code OKC·2009-03-04
K082047 — SECURACATH CATHETER, MODEL SPK01Code OKC·2008-09-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.