FDA 510(k)

Skypro, 外科手术服 6021

K号: K230707 · 2023-10-12

决定日期2023-10-12

产品代码FYA

咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。

决定实质等同

器械摘要

Skypro, Surgical Gown 6021 is the device name listed in this FDA 510(k) record. The listed applicant is Skypro Medical Supplies Company. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K230707. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Skypro, Surgical Gown 6021?

Skypro, Surgical Gown 6021 is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Skypro Medical Supplies Company. The 510(k) number is K230707.

When did Skypro, Surgical Gown 6021 receive FDA 510(k) clearance?

Skypro, Surgical Gown 6021 received FDA 510(k) clearance on 2023-10-12, under 510(k) number K230707.

Who is the listed applicant for Skypro, Surgical Gown 6021?

The FDA 510(k) record lists Skypro Medical Supplies Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Skypro, Surgical Gown 6021?

The FDA product code for Skypro, Surgical Gown 6021 is FYA.

列明Skypro Medical Supplies Company为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K202255Skypro, SP02 面罩（3）K152197Skypro, SP01 面罩

相关器械（代码：FYA）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K260407原理与意愿 ANSI/AAMI PB 70（无菌/非无菌）三级手术服（加固型）和原理与意愿 ANSI/AMMI PB70（无菌/非无菌）四级手术服/隔离服Principle & Will Co., Ltd.K261028手术服 Level2（S，M，L，XL，XXL，XXXL）Yadu Medical (Henan) Co., Ltd.K261949NYES Tuff Cuff L3 一次性隔离衣New York Embroidery Studio K252575Tuff Cuff™ 一次性手术服 AAMI L4 灭菌-大号（ML-L4-STL-DC-L）New York Embroidery Studio (NYES)K260725BAÜMER 手术服（COP01, COP04, COP05, COP10）Hindernis DE Mexico, S.A.P.I. DE C.V.K253243Cardinal Health™聚酯增强手术服Cardinal Health 200, LLC

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。