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FDA 510(k)

MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT

K-Number: K960983 · 1996-05-30

Decision Date1996-05-30
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronics Interventional Vascular. It received FDA 510(k) clearance on 1996-05-30 under 510(k) number K960983. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT?

MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K960983.

When did MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT receive FDA 510(k) clearance?

MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT received FDA 510(k) clearance on 1996-05-30, under 510(k) number K960983.

Who is the listed applicant for MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT?

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

What is the FDA product code for MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT?

The FDA product code for MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT is MAV.

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 Medtronics Interventional 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 21 devices →

Related Devices (Code: MAV)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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