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FDA 510(k)

VASCUMED EZ Y-CONNECTOR

K-Number: K902741 · 1990-11-01

ApplicantVascumed Systems
Decision Date1990-11-01
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCUMED EZ Y-CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Vascumed Systems. It received FDA 510(k) clearance on 1990-11-01 under 510(k) number K902741. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCUMED EZ Y-CONNECTOR?

VASCUMED EZ Y-CONNECTOR is a medical device that received FDA 510(k) clearance on 1990-11-01. The listed applicant is Vascumed Systems. The 510(k) number is K902741.

When did VASCUMED EZ Y-CONNECTOR receive FDA 510(k) clearance?

VASCUMED EZ Y-CONNECTOR received FDA 510(k) clearance on 1990-11-01, under 510(k) number K902741.

Who is the listed applicant for VASCUMED EZ Y-CONNECTOR?

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

What is the FDA product code for VASCUMED EZ Y-CONNECTOR?

The FDA product code for VASCUMED EZ Y-CONNECTOR is DTL.

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.

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Other records listing Vascumed Systems 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.

K903621MAGNUM-20 (TM) INFLATION DEVICE

Related Devices (Code: DTL)

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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