ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK
K-Number: K102648 · 2011-07-01
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Device Summary
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
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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