泰倫 NM-101
K 號：K230187 · 2023-09-29
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器材摘要
Terran NM-101 is the device name listed in this FDA 510(k) record. The listed applicant is Terran Biosciences, Inc.. It received FDA 510(k) clearance on 2023-09-29 under 510(k) number K230187. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Terran NM-101?
Terran NM-101 is a medical device that received FDA 510(k) clearance on 2023-09-29. The listed applicant is Terran Biosciences, Inc.. The 510(k) number is K230187.
When did Terran NM-101 receive FDA 510(k) clearance?
Terran NM-101 received FDA 510(k) clearance on 2023-09-29, under 510(k) number K230187.
Who is the listed applicant for Terran NM-101?
The FDA 510(k) record lists Terran Biosciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Terran NM-101?
The FDA product code for Terran NM-101 is LNH.
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相關器械（代碼：LNH）
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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