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FDA 510(k)

ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520

K-Number: K093050 · 2009-12-18

ApplicantArrow Intl., Inc.
Decision Date2009-12-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520 is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 2009-12-18 under 510(k) number K093050. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520?

ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520 is a medical device that received FDA 510(k) clearance on 2009-12-18. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K093050.

When did ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520 receive FDA 510(k) clearance?

ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520 received FDA 510(k) clearance on 2009-12-18, under 510(k) number K093050.

Who is the listed applicant for ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520?

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

What is the FDA product code for ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520?

The FDA product code for ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520 is DQY.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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