OncoPatch
K 號：K252296 · 2025-12-05
廣告
器材摘要
OncoPatch is the device name listed in this FDA 510(k) record. The listed applicant is Oncopatch, Inc.. It received FDA 510(k) clearance on 2025-12-05 under 510(k) number K252296. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the OncoPatch?
OncoPatch is a medical device that received FDA 510(k) clearance on 2025-12-05. The listed applicant is Oncopatch, Inc.. The 510(k) number is K252296.
When did OncoPatch receive FDA 510(k) clearance?
OncoPatch received FDA 510(k) clearance on 2025-12-05, under 510(k) number K252296.
Who is the listed applicant for OncoPatch?
The FDA 510(k) record lists Oncopatch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OncoPatch?
The FDA product code for OncoPatch is KXK.
相關臨床試驗
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。
相關器械（代碼：KXK）
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。
K242818IsoSphereIsoaid, LLCK223465RadianceTx 放射性同位素近端放射治療源Radiance Therapeutics, Inc.K221539伽馬TileGt Medical TechnologiesK202267Sirius MRI 標記，內含 Sirius MRI 標記的 Cs-131 預裝纖維，以 18 觀針製成Isoray Medical, Inc.K193602LV Liberty Vision 模型 1 90釔近端放射源Lv Liberty Vision CorporationK190839伽馬TileGt Medical Technologies
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
廣告