免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

LSSA (NP-200)

K号: K252495 · 2026-04-03

决定日期2026-04-03
产品代码QPB
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

LSSA (NP-200) is the device name listed in this FDA 510(k) record. The listed applicant is Newpong Co., Ltd.. It received FDA 510(k) clearance on 2026-04-03 under 510(k) number K252495. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LSSA (NP-200)?

LSSA (NP-200) is a medical device that received FDA 510(k) clearance on 2026-04-03. The listed applicant is Newpong Co., Ltd.. The 510(k) number is K252495.

When did LSSA (NP-200) receive FDA 510(k) clearance?

LSSA (NP-200) received FDA 510(k) clearance on 2026-04-03, under 510(k) number K252495.

Who is the listed applicant for LSSA (NP-200)?

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

What is the FDA product code for LSSA (NP-200)?

The FDA product code for LSSA (NP-200) is QPB.

相关器械(代码:QPB)

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。

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。

↑