顯微鏡下荧光雜交，17p染色體缺失（TP53）
PMA 核准號：P150041 · 2026-02-18
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器材摘要
Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Molecular, Inc.. It received FDA 510(k) clearance on 2026-02-18. The device is classified under product code PNK. It was reviewed by the PA advisory panel.
常見問題
What is the Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is a medical device that received FDA 510(k) clearance on 2026-02-18. The listed applicant is Abbott Molecular, Inc..
When did Fluorescence in situ hybridization, chromosome 17p deletion (TP53) receive FDA 510(k) clearance?
The clearance date for Fluorescence in situ hybridization, chromosome 17p deletion (TP53) can be found in the official FDA records.
Who is the listed applicant for Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
The FDA 510(k) record lists Abbott Molecular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
The FDA product code for Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is PNK.
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官方來源
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