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FDA 510(k)

ATS Y ADAPTER CODE #2452

K-Number: K900299 · 1990-05-01

ApplicantArtium Medical Corp.
Decision Date1990-05-01
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ATS Y ADAPTER CODE #2452 is the device name listed in this FDA 510(k) record. The listed applicant is Artium Medical Corp.. It received FDA 510(k) clearance on 1990-05-01 under 510(k) number K900299. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATS Y ADAPTER CODE #2452?

ATS Y ADAPTER CODE #2452 is a medical device that received FDA 510(k) clearance on 1990-05-01. The listed applicant is Artium Medical Corp.. The 510(k) number is K900299.

When did ATS Y ADAPTER CODE #2452 receive FDA 510(k) clearance?

ATS Y ADAPTER CODE #2452 received FDA 510(k) clearance on 1990-05-01, under 510(k) number K900299.

Who is the listed applicant for ATS Y ADAPTER CODE #2452?

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

What is the FDA product code for ATS Y ADAPTER CODE #2452?

The FDA product code for ATS Y ADAPTER CODE #2452 is CAC.

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Related Devices (Code: CAC)

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Official Source

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

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