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FDA 510(k)

VASCLIP

K-Number: K021745 · 2002-08-20

ApplicantVmbc, LLC
Decision Date2002-08-20
Product CodeNJC
Advisory CommitteeSU
DecisionUnknown

Device Summary

VASCLIP is the device name listed in this FDA 510(k) record. The listed applicant is Vmbc, LLC. It received FDA 510(k) clearance on 2002-08-20 under 510(k) number K021745. The device is classified under product code NJC. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VASCLIP?

VASCLIP is a medical device that received FDA 510(k) clearance on 2002-08-20. The listed applicant is Vmbc, LLC. The 510(k) number is K021745.

When did VASCLIP receive FDA 510(k) clearance?

VASCLIP received FDA 510(k) clearance on 2002-08-20, under 510(k) number K021745.

Who is the listed applicant for VASCLIP?

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

What is the FDA product code for VASCLIP?

The FDA product code for VASCLIP is NJC.

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.

Related Devices (Code: NJC)

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

View on FDA Database →

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

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