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FDA 510(k)

OXTI INFLATION DEVICE

K-Number: K122152 · 2012-12-14

Decision Date2012-12-14
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXTI INFLATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Oxti Corporation. It received FDA 510(k) clearance on 2012-12-14 under 510(k) number K122152. 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 OXTI INFLATION DEVICE?

OXTI INFLATION DEVICE is a medical device that received FDA 510(k) clearance on 2012-12-14. The listed applicant is Oxti Corporation. The 510(k) number is K122152.

When did OXTI INFLATION DEVICE receive FDA 510(k) clearance?

OXTI INFLATION DEVICE received FDA 510(k) clearance on 2012-12-14, under 510(k) number K122152.

Who is the listed applicant for OXTI INFLATION DEVICE?

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

What is the FDA product code for OXTI INFLATION DEVICE?

The FDA product code for OXTI 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.

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

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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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