FDA 510(k)

SECURACATH UNIVERSAL

K-Number: K092306 · 2010-07-09

Decision Date2010-07-09

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SECURACATH UNIVERSAL is the device name listed in this FDA 510(k) record. The listed applicant is Interrad Medical, Inc.. It received FDA 510(k) clearance on 2010-07-09 under 510(k) number K092306. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECURACATH UNIVERSAL?

SECURACATH UNIVERSAL is a medical device that received FDA 510(k) clearance on 2010-07-09. The listed applicant is Interrad Medical, Inc.. The 510(k) number is K092306.

When did SECURACATH UNIVERSAL receive FDA 510(k) clearance?

SECURACATH UNIVERSAL received FDA 510(k) clearance on 2010-07-09, under 510(k) number K092306.

Who is the listed applicant for SECURACATH UNIVERSAL?

The FDA 510(k) record lists Interrad Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SECURACATH UNIVERSAL?

The FDA product code for SECURACATH UNIVERSAL is LJS.

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Other records listing Interrad Medical, Inc. as applicant

K210629SecurAcath K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F K180769SecurAcath K120935SECURACATH K083081MODIFICATION TO SECURACATH, MODEL: SPK01 K082047SECURACATH CATHETER, MODEL SPK01

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Related Devices (Code: LJS)

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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.