SecurAcath
K-Number: K210629 · 2021-04-12
ApplicantInterrad Medical, Inc.
Decision Date2021-04-12
Product CodeOKC
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
SecurAcath is a medical device manufactured by Interrad Medical, Inc.. It received FDA 510(k) clearance on 2021-04-12 under approval number K210629. The device is classified under product code OKC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SecurAcath?
SecurAcath is a medical device that received FDA 510(k) clearance on 2021-04-12. It is manufactured by Interrad Medical, Inc.. The 510(k) number is K210629.
When was SecurAcath approved by the FDA?
SecurAcath received FDA 510(k) clearance on 2021-04-12, under approval number K210629.
What company makes SecurAcath?
SecurAcath is manufactured by Interrad Medical, Inc..
What is the FDA product code for SecurAcath?
The FDA product code for SecurAcath is OKC.
Other Devices by Interrad Medical, Inc.
Related Devices (Code: OKC)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.