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FDA 510(k)

MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

K-Number: K953564 · 1996-02-02

ApplicantMedtronic Cardiac Surgery, Medtronic, Inc.
Decision Date1996-02-02
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Cardiac Surgery, Medtronic, Inc.. It received FDA 510(k) clearance on 1996-02-02 under 510(k) number K953564. 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 MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE?

MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE is a medical device that received FDA 510(k) clearance on 1996-02-02. The listed applicant is Medtronic Cardiac Surgery, Medtronic, Inc.. The 510(k) number is K953564.

When did MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE receive FDA 510(k) clearance?

MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE received FDA 510(k) clearance on 1996-02-02, under 510(k) number K953564.

Who is the listed applicant for MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE?

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

What is the FDA product code for MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE?

The FDA product code for MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE is DTL.

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Other records listing Medtronic Cardiac Surgery, Medtronic, 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.

K960755CARDIOTHERM BLOOD CARDIOPLEGIA SYSTEMS

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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