FDA 510(k)

CorVision® (91-205-Z0014)

K 號：K260051 · 2026-05-12

決定日期2026-05-12

產品代碼MOD

諮詢委員會AN

決定相當於

器材摘要

CorVision® (91-205-Z0014) is the device name listed in this FDA 510(k) record. The listed applicant is CorVent® Medical, Inc.. It received FDA 510(k) clearance on 2026-05-12 under 510(k) number K260051. The device is classified under product code MOD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CorVision® (91-205-Z0014)?

CorVision® (91-205-Z0014) is a medical device that received FDA 510(k) clearance on 2026-05-12. The listed applicant is CorVent® Medical, Inc.. The 510(k) number is K260051.

When did CorVision® (91-205-Z0014) receive FDA 510(k) clearance?

CorVision® (91-205-Z0014) received FDA 510(k) clearance on 2026-05-12, under 510(k) number K260051.

Who is the listed applicant for CorVision® (91-205-Z0014)?

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

What is the FDA product code for CorVision® (91-205-Z0014)?

The FDA product code for CorVision® (91-205-Z0014) is MOD.

其他以 CorVent® Medical, Inc. 為申請人之記錄

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K241135RESPOND(R) 呼吸器

相關器械（代碼：MOD）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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