FDA 510(k)

Copioumed AAMI 3外科手术服

K号: K251860 · 2026-02-26

决定日期2026-02-26

产品代码FYA

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决定实质等同

器械摘要

Copioumed AAMI 3 Surgical Gown is the device name listed in this FDA 510(k) record. The listed applicant is Copioumed International, Inc.. It received FDA 510(k) clearance on 2026-02-26 under 510(k) number K251860. 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 Copioumed AAMI 3 Surgical Gown?

Copioumed AAMI 3 Surgical Gown is a medical device that received FDA 510(k) clearance on 2026-02-26. The listed applicant is Copioumed International, Inc.. The 510(k) number is K251860.

When did Copioumed AAMI 3 Surgical Gown receive FDA 510(k) clearance?

Copioumed AAMI 3 Surgical Gown received FDA 510(k) clearance on 2026-02-26, under 510(k) number K251860.

Who is the listed applicant for Copioumed AAMI 3 Surgical Gown?

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

What is the FDA product code for Copioumed AAMI 3 Surgical Gown?

The FDA product code for Copioumed AAMI 3 Surgical Gown is FYA.

列明Copioumed International, Inc.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。

K230135Copioumed 化疗隔离服

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

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