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FDA 510(k)

Guidewire Locking Device

K-Number: K220247 · 2022-03-29

ApplicantMicro-Tech (Nanjing) Co., Ltd.
Decision Date2022-03-29
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Guidewire Locking Device is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2022-03-29 under approval number K220247. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Guidewire Locking Device?

Guidewire Locking Device is a medical device that received FDA 510(k) clearance on 2022-03-29. It is manufactured by Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K220247.

When was Guidewire Locking Device approved by the FDA?

Guidewire Locking Device received FDA 510(k) clearance on 2022-03-29, under approval number K220247.

What company makes Guidewire Locking Device?

Guidewire Locking Device is manufactured by Micro-Tech (Nanjing) Co., Ltd..

What is the FDA product code for Guidewire Locking Device?

The FDA product code for Guidewire Locking Device is ODC.

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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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