FDA 510(k)

MD床墊縫合位置設備

K 號：K222783 · 2024-01-12

決定日期2024-01-12

產品代碼GCJ

諮詢委員會GU

決定相當於

器材摘要

MD Mattress Suture Placement Device is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2024-01-12 under 510(k) number K222783. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MD Mattress Suture Placement Device?

MD Mattress Suture Placement Device is a medical device that received FDA 510(k) clearance on 2024-01-12. The listed applicant is Lsi Solutions, Inc.. The 510(k) number is K222783.

When did MD Mattress Suture Placement Device receive FDA 510(k) clearance?

MD Mattress Suture Placement Device received FDA 510(k) clearance on 2024-01-12, under 510(k) number K222783.

Who is the listed applicant for MD Mattress Suture Placement Device?

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

What is the FDA product code for MD Mattress Suture Placement Device?

The FDA product code for MD Mattress Suture Placement Device is GCJ.

其他以 Lsi Solutions, Inc. 為申請人之記錄

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。

K202551科結微 K203120RD快速上縫針，0聚酯，RD快速上縫針，2-0聚酯，RD QUCIK LOAD SUTURE，2-0聚丙烯

相關器械（代碼：GCJ）

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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