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FDA 510(k)

Freespira 呼吸系統

K 號:K233337 · 2025-04-24

決定日期2025-04-24
產品代碼SEN
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Freespira Breathing System is the device name listed in this FDA 510(k) record. The listed applicant is Freespira, Inc.. It received FDA 510(k) clearance on 2025-04-24 under 510(k) number K233337. The device is classified under product code SEN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Freespira Breathing System?

Freespira Breathing System is a medical device that received FDA 510(k) clearance on 2025-04-24. The listed applicant is Freespira, Inc.. The 510(k) number is K233337.

When did Freespira Breathing System receive FDA 510(k) clearance?

Freespira Breathing System received FDA 510(k) clearance on 2025-04-24, under 510(k) number K233337.

Who is the listed applicant for Freespira Breathing System?

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

What is the FDA product code for Freespira Breathing System?

The FDA product code for Freespira Breathing System is SEN.

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