Disposable Dual Action Tissue Clip
K-Number: K212748 · 2022-01-20
ApplicantMicro-Tech (Nanjing) Co., Ltd.
Decision Date2022-01-20
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Disposable Dual Action Tissue Clip is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2022-01-20 under approval 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. It is manufactured by Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K212748.
When was Disposable Dual Action Tissue Clip approved by the FDA?
Disposable Dual Action Tissue Clip received FDA 510(k) clearance on 2022-01-20, under approval number K212748.
What company makes Disposable Dual Action Tissue Clip?
Disposable Dual Action Tissue Clip is manufactured by Micro-Tech (Nanjing) Co., Ltd..
What is the FDA product code for Disposable Dual Action Tissue Clip?
The FDA product code for Disposable Dual Action Tissue Clip is PKL.
Related PubMed Literature
Other Devices by Micro-Tech (Nanjing) Co., Ltd.
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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.