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FDA 510(k)

ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK

K-Number: K102648 · 2011-07-01

Decision Date2011-07-01
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Ant Hi-Tech Industrial Co., Ltd.. It received FDA 510(k) clearance on 2011-07-01 under 510(k) number K102648. 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 ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK?

ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK is a medical device that received FDA 510(k) clearance on 2011-07-01. The listed applicant is Shenzhen Ant Hi-Tech Industrial Co., Ltd.. The 510(k) number is K102648.

When did ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK receive FDA 510(k) clearance?

ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK received FDA 510(k) clearance on 2011-07-01, under 510(k) number K102648.

Who is the listed applicant for ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK?

The FDA 510(k) record lists Shenzhen Ant Hi-Tech Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK?

The FDA product code for ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK 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 Shenzhen Ant Hi-Tech Industrial Co., Ltd. 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

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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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