Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDFLATOR INFLATION SYSTEM

K-Number: K910958 · 1991-07-12

ApplicantMedex, Inc.
Decision Date1991-07-12
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDFLATOR INFLATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1991-07-12 under 510(k) number K910958. 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 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.

View all 48 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.

↑