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FDA 510(k)

MERCATOR MICROSYRINGE II INFUSION CATHETER

K-Number: K062752 · 2006-12-07

Decision Date2006-12-07
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MERCATOR MICROSYRINGE II INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Mercator Medsystems, Inc.. It received FDA 510(k) clearance on 2006-12-07 under 510(k) number K062752. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCATOR MICROSYRINGE II INFUSION CATHETER?

MERCATOR MICROSYRINGE II INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 2006-12-07. The listed applicant is Mercator Medsystems, Inc.. The 510(k) number is K062752.

When did MERCATOR MICROSYRINGE II INFUSION CATHETER receive FDA 510(k) clearance?

MERCATOR MICROSYRINGE II INFUSION CATHETER received FDA 510(k) clearance on 2006-12-07, under 510(k) number K062752.

Who is the listed applicant for MERCATOR MICROSYRINGE II INFUSION CATHETER?

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

What is the FDA product code for MERCATOR MICROSYRINGE II INFUSION CATHETER?

The FDA product code for MERCATOR MICROSYRINGE II INFUSION CATHETER is KRA.

Related Clinical Trials

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.

Other records listing Mercator Medsystems, 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.

Related Devices (Code: KRA)

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.

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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