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FDA 510(k)

MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE

K-Number: K874117 · 1987-11-05

Decision Date1987-11-05
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-11-05 under 510(k) number K874117. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE?

MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE is a medical device that received FDA 510(k) clearance on 1987-11-05. The listed applicant is Medtronic Vascular. The 510(k) number is K874117.

When did MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE receive FDA 510(k) clearance?

MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE received FDA 510(k) clearance on 1987-11-05, under 510(k) number K874117.

Who is the listed applicant for MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE?

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

What is the FDA product code for MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE?

The FDA product code for MEDTRONIC MODEL 6550 ADJUSTABLE HEMOSTASIS VALVE is DYG.

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.

Other records listing Medtronic Vascular 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.

View all 474 devices →

Related Devices (Code: DYG)

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

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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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