FDA 510(k)

足跟棒安全刀片（HHZ-II，HHZ-III，HHZ-IV）

K号: K252490 · 2026-02-12

决定日期2026-02-12

产品代码FMK

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决定实质等同

器械摘要

Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV) is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Huahong Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-12 under 510(k) number K252490. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)?

Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV) is a medical device that received FDA 510(k) clearance on 2026-02-12. The listed applicant is Tianjin Huahong Technology Co., Ltd.. The 510(k) number is K252490.

When did Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV) receive FDA 510(k) clearance?

Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV) received FDA 510(k) clearance on 2026-02-12, under 510(k) number K252490.

Who is the listed applicant for Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)?

FDA 510(k)记录将天津华宏科技有限公司列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)?

The FDA product code for Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV) is FMK.

列明Tianjin Huahong Technology Co., Ltd.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。

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官方来源

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