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FDA 510(k)

ACUNAV V ULTRASOUND CATHETER

K-Number: K081808 · 2008-09-26

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2008-09-26
Product CodeOBJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACUNAV V ULTRASOUND CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2008-09-26 under 510(k) number K081808. The device is classified under product code OBJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUNAV V ULTRASOUND CATHETER?

ACUNAV V ULTRASOUND CATHETER is a medical device that received FDA 510(k) clearance on 2008-09-26. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K081808.

When did ACUNAV V ULTRASOUND CATHETER receive FDA 510(k) clearance?

ACUNAV V ULTRASOUND CATHETER received FDA 510(k) clearance on 2008-09-26, under 510(k) number K081808.

Who is the listed applicant for ACUNAV V ULTRASOUND CATHETER?

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

What is the FDA product code for ACUNAV V ULTRASOUND CATHETER?

The FDA product code for ACUNAV V ULTRASOUND CATHETER is OBJ.

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Related Devices (Code: OBJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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