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FDA 510(k)

MULTICROSS SUPPORT CATHETER

K-Number: K121763 · 2012-11-27

ApplicantRoxwood Medical, Inc.
Decision Date2012-11-27
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTICROSS SUPPORT CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Roxwood Medical, Inc.. It received FDA 510(k) clearance on 2012-11-27 under 510(k) number K121763. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICROSS SUPPORT CATHETER?

MULTICROSS SUPPORT CATHETER is a medical device that received FDA 510(k) clearance on 2012-11-27. The listed applicant is Roxwood Medical, Inc.. The 510(k) number is K121763.

When did MULTICROSS SUPPORT CATHETER receive FDA 510(k) clearance?

MULTICROSS SUPPORT CATHETER received FDA 510(k) clearance on 2012-11-27, under 510(k) number K121763.

Who is the listed applicant for MULTICROSS SUPPORT CATHETER?

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

What is the FDA product code for MULTICROSS SUPPORT CATHETER?

The FDA product code for MULTICROSS SUPPORT CATHETER is DQY.

Related Clinical Trials

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Other records listing Roxwood Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: DQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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