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FDA 510(k)

GRI-Alleset Veress Needle

K-Number: K172835 · 2018-06-11

ApplicantGri Medical and Electronic Technology Co., Ltd.
Decision Date2018-06-11
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Gri Medical and Electronic Technology Co., Ltd.. The 510(k) number is K172835.

When was GRI-Alleset Veress Needle approved by the FDA?

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

What company makes GRI-Alleset Veress Needle?

GRI-Alleset Veress Needle is manufactured by Gri Medical and Electronic Technology Co., Ltd..

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

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

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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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