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FDA 510(k)

Single Use Grasping Forceps

K-Number: K191900 · 2020-03-27

ApplicantZhejiang Chuangxiang Medical Technology Co., Ltd.
Decision Date2020-03-27
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single Use Grasping Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-03-27 under 510(k) number K191900. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Grasping Forceps?

Single Use Grasping Forceps is a medical device that received FDA 510(k) clearance on 2020-03-27. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K191900.

When did Single Use Grasping Forceps receive FDA 510(k) clearance?

Single Use Grasping Forceps received FDA 510(k) clearance on 2020-03-27, under 510(k) number K191900.

Who is the listed applicant for Single Use Grasping Forceps?

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

What is the FDA product code for Single Use Grasping Forceps?

The FDA product code for Single Use Grasping Forceps is OCZ.

Other records listing Zhejiang Chuangxiang Medical Technology Co., Ltd. as applicant

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Related Devices (Code: OCZ)

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.

K252800KARL STORZ Endoscopic Accessories for UrologyKarl Storz SE & CO. KGK242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter (SC500230)Envision EndoscopyK152802Grasping ForcepsMicro-Tech (Nanjing) Co., Ltd.

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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