FDA 510(k)

SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle

Número K: K151069 · 2016-02-05

Data da decisão2016-02-05

Código do produtoBSP

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle is the device name listed in this FDA 510(k) record. The listed applicant is Spectra Medical Devices, Inc.. It received FDA 510(k) clearance on 2016-02-05 under 510(k) number K151069. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle?

SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle is a medical device that received FDA 510(k) clearance on 2016-02-05. The listed applicant is Spectra Medical Devices, Inc.. The 510(k) number is K151069.

When did SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle receive FDA 510(k) clearance?

SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle received FDA 510(k) clearance on 2016-02-05, under 510(k) number K151069.

Who is the listed applicant for SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle?

The FDA 510(k) record lists Spectra Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle?

The FDA product code for SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle is BSP.

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