MEDTRONIC EVEREST INFLATION DEVICE
K-Number: K942269 · 1994-10-18
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Device Summary
Frequently Asked Questions
What is the MEDTRONIC EVEREST INFLATION DEVICE?
MEDTRONIC EVEREST INFLATION DEVICE is a medical device that received FDA 510(k) clearance on 1994-10-18. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K942269.
When did MEDTRONIC EVEREST INFLATION DEVICE receive FDA 510(k) clearance?
MEDTRONIC EVEREST INFLATION DEVICE received FDA 510(k) clearance on 1994-10-18, under 510(k) number K942269.
Who is the listed applicant for MEDTRONIC EVEREST INFLATION DEVICE?
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 EVEREST INFLATION DEVICE?
The FDA product code for MEDTRONIC EVEREST INFLATION DEVICE 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.
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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