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FDA 510(k)

A-V FOOT PUMP

K-Number: K121718 · 2012-08-17

Decision Date2012-08-17
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A-V FOOT PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Dalian Labtek Science & Development Co., Ltd.. It received FDA 510(k) clearance on 2012-08-17 under 510(k) number K121718. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-V FOOT PUMP?

A-V FOOT PUMP is a medical device that received FDA 510(k) clearance on 2012-08-17. The listed applicant is Dalian Labtek Science & Development Co., Ltd.. The 510(k) number is K121718.

When did A-V FOOT PUMP receive FDA 510(k) clearance?

A-V FOOT PUMP received FDA 510(k) clearance on 2012-08-17, under 510(k) number K121718.

Who is the listed applicant for A-V FOOT PUMP?

The FDA 510(k) record lists Dalian Labtek Science & Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-V FOOT PUMP?

The FDA product code for A-V FOOT PUMP is JOW.

Other records listing Dalian Labtek Science & Development 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: JOW)

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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