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FDA 510(k)

VEIN ENTRY INDICATOR DEVICE (VEID)

K-Number: K993995 · 2000-02-14

ApplicantVascular Technologies , Ltd.
Decision Date2000-02-14
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VEIN ENTRY INDICATOR DEVICE (VEID) is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technologies , Ltd.. It received FDA 510(k) clearance on 2000-02-14 under 510(k) number K993995. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEIN ENTRY INDICATOR DEVICE (VEID)?

VEIN ENTRY INDICATOR DEVICE (VEID) is a medical device that received FDA 510(k) clearance on 2000-02-14. The listed applicant is Vascular Technologies , Ltd.. The 510(k) number is K993995.

When did VEIN ENTRY INDICATOR DEVICE (VEID) receive FDA 510(k) clearance?

VEIN ENTRY INDICATOR DEVICE (VEID) received FDA 510(k) clearance on 2000-02-14, under 510(k) number K993995.

Who is the listed applicant for VEIN ENTRY INDICATOR DEVICE (VEID)?

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

What is the FDA product code for VEIN ENTRY INDICATOR DEVICE (VEID)?

The FDA product code for VEIN ENTRY INDICATOR DEVICE (VEID) is FMF.

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Related Devices (Code: FMF)

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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