Pre-B Seal肺活检塞系统 - 15cm型号(FG0001);Pre-B Seal肺活检塞系统 - 16cm型号(FG0002);Pre-B Seal肺活检塞系统 - 20cm型号(FG0003)
K号: K243722 · 2025-04-08
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器械摘要
常见问题
What is the Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003)?
Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003) is a medical device that received FDA 510(k) clearance on 2025-04-08. The listed applicant is Selio Medical Limited. The 510(k) number is K243722.
When did Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003) receive FDA 510(k) clearance?
Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003) received FDA 510(k) clearance on 2025-04-08, under 510(k) number K243722.
Who is the listed applicant for Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003)?
The FDA 510(k) record lists Selio Medical Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003)?
The FDA product code for Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003) is OMT.
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