Disposable Dual Action Tissue Clip
K-Number: K212748 · 2022-01-20
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.