FDA 510(k)

PMT Platinum Depthalon Depth Electrode

Número K: K151790 · 2016-07-14

Data da decisão2016-07-14

Código do produtoGZL

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

PMT Platinum Depthalon Depth Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corporation. It received FDA 510(k) clearance on 2016-07-14 under 510(k) number K151790. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the PMT Platinum Depthalon Depth Electrode?

PMT Platinum Depthalon Depth Electrode is a medical device that received FDA 510(k) clearance on 2016-07-14. The listed applicant is Pmt Corporation. The 510(k) number is K151790.

When did PMT Platinum Depthalon Depth Electrode receive FDA 510(k) clearance?

PMT Platinum Depthalon Depth Electrode received FDA 510(k) clearance on 2016-07-14, under 510(k) number K151790.

Who is the listed applicant for PMT Platinum Depthalon Depth Electrode?

The FDA 510(k) record lists Pmt Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMT Platinum Depthalon Depth Electrode?

The FDA product code for PMT Platinum Depthalon Depth Electrode is GZL.

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Dispositivos Relacionados (Código: GZL)

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