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FDA 510(k)

WELLGRAFT PE I

K-Number: K072444 · 2008-04-04

ApplicantGwowei Technology Co., Ltd.
Decision Date2008-04-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WELLGRAFT PE I is the device name listed in this FDA 510(k) record. The listed applicant is Gwowei Technology Co., Ltd.. It received FDA 510(k) clearance on 2008-04-04 under 510(k) number K072444. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELLGRAFT PE I?

WELLGRAFT PE I is a medical device that received FDA 510(k) clearance on 2008-04-04. The listed applicant is Gwowei Technology Co., Ltd.. The 510(k) number is K072444.

When did WELLGRAFT PE I receive FDA 510(k) clearance?

WELLGRAFT PE I received FDA 510(k) clearance on 2008-04-04, under 510(k) number K072444.

Who is the listed applicant for WELLGRAFT PE I?

The FDA 510(k) record lists Gwowei Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WELLGRAFT PE I?

The FDA product code for WELLGRAFT PE I is MQV.

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.

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Other records listing Gwowei Technology 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.

K072170WELLGRAFT PE II

Related Devices (Code: MQV)

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.

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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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