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FDA 510(k)

VP-2000/1000

K-Number: K013434 · 2002-07-09

ApplicantColin Corp.
Decision Date2002-07-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VP-2000/1000 is the device name listed in this FDA 510(k) record. The listed applicant is Colin Corp.. It received FDA 510(k) clearance on 2002-07-09 under 510(k) number K013434. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VP-2000/1000?

VP-2000/1000 is a medical device that received FDA 510(k) clearance on 2002-07-09. The listed applicant is Colin Corp.. The 510(k) number is K013434.

When did VP-2000/1000 receive FDA 510(k) clearance?

VP-2000/1000 received FDA 510(k) clearance on 2002-07-09, under 510(k) number K013434.

Who is the listed applicant for VP-2000/1000?

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

What is the FDA product code for VP-2000/1000?

The FDA product code for VP-2000/1000 is DXN.

Related Devices (Code: DXN)

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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