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FDA 510(k)

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL)

K-Number: K121667 · 2012-08-13

Decision Date2012-08-13
Product CodeLOX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2012-08-13 under 510(k) number K121667. The device is classified under product code LOX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL)?

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) is a medical device that received FDA 510(k) clearance on 2012-08-13. The listed applicant is Boston Scientific Corp. The 510(k) number is K121667.

When did NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) receive FDA 510(k) clearance?

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) received FDA 510(k) clearance on 2012-08-13, under 510(k) number K121667.

Who is the listed applicant for NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL)?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL)?

The FDA product code for NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) is LOX.

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 Boston Scientific Corp 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: LOX)

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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