FDA 510(k)

Lawson Retrograde Nephrostomy Wire Puncture Set

Número K: K190903 · 2019-12-16

Data da decisão2019-12-16

Código do produtoLJE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Lawson Retrograde Nephrostomy Wire Puncture Set is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2019-12-16 under 510(k) number K190903. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Lawson Retrograde Nephrostomy Wire Puncture Set?

Lawson Retrograde Nephrostomy Wire Puncture Set is a medical device that received FDA 510(k) clearance on 2019-12-16. The listed applicant is Cook Incorporated. The 510(k) number is K190903.

When did Lawson Retrograde Nephrostomy Wire Puncture Set receive FDA 510(k) clearance?

Lawson Retrograde Nephrostomy Wire Puncture Set received FDA 510(k) clearance on 2019-12-16, under 510(k) number K190903.

Who is the listed applicant for Lawson Retrograde Nephrostomy Wire Puncture Set?

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

What is the FDA product code for Lawson Retrograde Nephrostomy Wire Puncture Set?

The FDA product code for Lawson Retrograde Nephrostomy Wire Puncture Set is LJE.

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Fonte oficial

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