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FDA 510(k)

雙重玻尿酸陰道栓劑(HA 5 mg);雙重玻尿酸陰道栓劑(HA 10 mg)

K 號:K260007 · 2026-04-01

決定日期2026-04-01
產品代碼NUC
諮詢委員會OB設備之醫療設備規範文本翻譯如下: 關於OB設備的醫療設備規範文件: 此設備已通過FDA認證,並獲得510(k)許可證。該設備的PMA申請已提交,並在NCT登錄編號為[編號]的研究中進行測試。相關文獻的PMID編號為[編號]。請參考以下識別碼和網址: 識別碼:[識別碼] 網址:[網址] 政策:醫療規範-v1
決定相當於

器材摘要

Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) is the device name listed in this FDA 510(k) record. The listed applicant is Hudi Pharma Srl. It received FDA 510(k) clearance on 2026-04-01 under 510(k) number K260007. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg)?

Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) is a medical device that received FDA 510(k) clearance on 2026-04-01. The listed applicant is Hudi Pharma Srl. The 510(k) number is K260007.

When did Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) receive FDA 510(k) clearance?

Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) received FDA 510(k) clearance on 2026-04-01, under 510(k) number K260007.

Who is the listed applicant for Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg)?

The FDA 510(k) record lists Hudi Pharma Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg)?

The FDA product code for Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) is NUC.

相關臨床試驗

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相關器械(代碼:NUC)

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。

官方來源

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