FDA 510(k)

B&J DVT Calf/Thigh Garments, Models 801/830 Series

Número K: K201532 · 2020-09-19

Data da decisão2020-09-19

Código do produtoJOW

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

B&J DVT Calf/Thigh Garments, Models 801/830 Series is the device name listed in this FDA 510(k) record. The listed applicant is B&J Manufacturing , Ltd.. It received FDA 510(k) clearance on 2020-09-19 under 510(k) number K201532. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the B&J DVT Calf/Thigh Garments, Models 801/830 Series?

B&J DVT Calf/Thigh Garments, Models 801/830 Series is a medical device that received FDA 510(k) clearance on 2020-09-19. The listed applicant is B&J Manufacturing , Ltd.. The 510(k) number is K201532.

When did B&J DVT Calf/Thigh Garments, Models 801/830 Series receive FDA 510(k) clearance?

B&J DVT Calf/Thigh Garments, Models 801/830 Series received FDA 510(k) clearance on 2020-09-19, under 510(k) number K201532.

Who is the listed applicant for B&J DVT Calf/Thigh Garments, Models 801/830 Series?

The FDA 510(k) record lists B&J Manufacturing , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B&J DVT Calf/Thigh Garments, Models 801/830 Series?

The FDA product code for B&J DVT Calf/Thigh Garments, Models 801/830 Series is JOW.

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Outros registros que listam B&J Manufacturing , Ltd. como candidato(a)

K201547B&J DVT Foot Garments, Models 820 Series K200568B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System K200154B&J DVT Compression Devices MHH800/MHH800SQ

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Fonte oficial

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