MEDFLATOR INFLATION SYSTEM
K-Number: K910958 · 1991-07-12
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Device Summary
Frequently Asked Questions
What is the MEDFLATOR INFLATION SYSTEM?
MEDFLATOR INFLATION SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-12. The listed applicant is Medex, Inc.. The 510(k) number is K910958.
When did MEDFLATOR INFLATION SYSTEM receive FDA 510(k) clearance?
MEDFLATOR INFLATION SYSTEM received FDA 510(k) clearance on 1991-07-12, under 510(k) number K910958.
Who is the listed applicant for MEDFLATOR INFLATION SYSTEM?
The FDA 510(k) record lists Medex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDFLATOR INFLATION SYSTEM?
The FDA product code for MEDFLATOR INFLATION SYSTEM 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 Medex, 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.
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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