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FDA 510(k)

RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set

Número K: K160077 · 2016-07-12

RequerenteJbw7 Innovations, LLC
Data da decisão2016-07-12
Código do produtoLJE
DecisãoSubstantially Equivalent

Resumo do dispositivo

RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set is the device name listed in this FDA 510(k) record. The listed applicant is Jbw7 Innovations, LLC. It received FDA 510(k) clearance on 2016-07-12 under 510(k) number K160077. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set?

RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set is a medical device that received FDA 510(k) clearance on 2016-07-12. The listed applicant is Jbw7 Innovations, LLC. The 510(k) number is K160077.

When did RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set receive FDA 510(k) clearance?

RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set received FDA 510(k) clearance on 2016-07-12, under 510(k) number K160077.

Who is the listed applicant for RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set?

The FDA 510(k) record lists Jbw7 Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set?

The FDA product code for RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set is LJE.

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Dispositivos Relacionados (Código: LJE)

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Fonte oficial

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