FDA 510(k)

Catasyn Advanced Technology Wound Hydrogel

K号: K172338 · 2018-02-21

决定日期2018-02-21

产品代码FRO

决定实质等同

器械摘要

Catasyn Advanced Technology Wound Hydrogel is the device name listed in this FDA 510(k) record. The listed applicant is Synedgen, Inc.. It received FDA 510(k) clearance on 2018-02-21 under 510(k) number K172338. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常见问题

What is the Catasyn Advanced Technology Wound Hydrogel?

Catasyn Advanced Technology Wound Hydrogel is a medical device that received FDA 510(k) clearance on 2018-02-21. The listed applicant is Synedgen, Inc.. The 510(k) number is K172338.

When did Catasyn Advanced Technology Wound Hydrogel receive FDA 510(k) clearance?

Catasyn Advanced Technology Wound Hydrogel received FDA 510(k) clearance on 2018-02-21, under 510(k) number K172338.

Who is the listed applicant for Catasyn Advanced Technology Wound Hydrogel?

The FDA 510(k) record lists Synedgen, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Catasyn Advanced Technology Wound Hydrogel?

The FDA product code for Catasyn Advanced Technology Wound Hydrogel is FRO. This falls under the Anesthesiology category.

列明Synedgen, Inc.为申报人的其他记录

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K193336Synvaza 口腔溃疡和伤口冲洗剂，Synvaza II 口腔溃疡和伤口冲洗剂

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