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FDA 510(k)

Arrow Seldinger Arterial Catheterisierungsgerät 18 ga., Arrow Seldinger Arterial Catheterisierungsgerät 20 ga., Arrow Seldinger Arterial Catheterisierungsgerät 22 ga., Arrow Seldinger Arterial Catheterisierungsgerät 24 ga.

K-Nummer: K171146 · 2017-06-23

AntragstellerArrow International, Inc. (Subsidiary of Telelflex Inc.)
Entscheidungsdatum2017-06-23
ProduktcodeDQY
BeratungsausschussCV
EntscheidungSubstantially Equivalent

Produktübersicht

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc. (Subsidiary of Telelflex Inc.). It received FDA 510(k) clearance on 2017-06-23 under 510(k) number K171146. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is a medical device that received FDA 510(k) clearance on 2017-06-23. The listed applicant is Arrow International, Inc. (Subsidiary of Telelflex Inc.). The 510(k) number is K171146.

When did Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. receive FDA 510(k) clearance?

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. received FDA 510(k) clearance on 2017-06-23, under 510(k) number K171146.

Who is the listed applicant for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

The FDA 510(k) record lists Arrow International, Inc. (Subsidiary of Telelflex Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

The FDA product code for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is DQY.

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Verwandte Geräte (Code: DQY)

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

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