FDA 510(k)

GRI-Alleset Veress 针

K号: K172835 · 2018-06-11

申请人Gri Medical and Electronic Technology Co., Ltd.

决定日期2018-06-11

产品代码HIF

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决定实质等同

器械摘要

GRI-Alleset Veress Needle is the device name listed in this FDA 510(k) record. The listed applicant is Gri Medical and Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-06-11 under 510(k) number K172835. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the GRI-Alleset Veress Needle?

GRI-Alleset Veress Needle is a medical device that received FDA 510(k) clearance on 2018-06-11. The listed applicant is Gri Medical and Electronic Technology Co., Ltd.. The 510(k) number is K172835.

When did GRI-Alleset Veress Needle receive FDA 510(k) clearance?

GRI-Alleset Veress Needle received FDA 510(k) clearance on 2018-06-11, under 510(k) number K172835.

Who is the listed applicant for GRI-Alleset Veress Needle?

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

What is the FDA product code for GRI-Alleset Veress Needle?

The FDA product code for GRI-Alleset Veress Needle is HIF.

列明Gri Medical and Electronic Technology Co., Ltd.为申报人的其他记录

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