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FDA 510(k)

THE V-BAG

K-Number: K001822 · 2000-07-07

ApplicantCirculatory Technology, Inc.
Decision Date2000-07-07
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE V-BAG is the device name listed in this FDA 510(k) record. The listed applicant is Circulatory Technology, Inc.. It received FDA 510(k) clearance on 2000-07-07 under 510(k) number K001822. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE V-BAG?

THE V-BAG is a medical device that received FDA 510(k) clearance on 2000-07-07. The listed applicant is Circulatory Technology, Inc.. The 510(k) number is K001822.

When did THE V-BAG receive FDA 510(k) clearance?

THE V-BAG received FDA 510(k) clearance on 2000-07-07, under 510(k) number K001822.

Who is the listed applicant for THE V-BAG?

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

What is the FDA product code for THE V-BAG?

The FDA product code for THE V-BAG is DTN.

Other records listing Circulatory Technology, 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: DTN)

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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