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FDA 510(k)

Disposable Dual Action Tissue Clip

K-Number: K212748 · 2022-01-20

Decision Date2022-01-20
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Disposable Dual Action Tissue Clip is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2022-01-20 under 510(k) number K212748. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Dual Action Tissue Clip?

Disposable Dual Action Tissue Clip is a medical device that received FDA 510(k) clearance on 2022-01-20. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K212748.

When did Disposable Dual Action Tissue Clip receive FDA 510(k) clearance?

Disposable Dual Action Tissue Clip received FDA 510(k) clearance on 2022-01-20, under 510(k) number K212748.

Who is the listed applicant for Disposable Dual Action Tissue Clip?

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

What is the FDA product code for Disposable Dual Action Tissue Clip?

The FDA product code for Disposable Dual Action Tissue Clip is PKL.

Other records listing Micro-Tech (Nanjing) 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.

View all 37 devices →

Related Devices (Code: PKL)

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.