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FDA 510(k)

EXPRESS AND OASIS CHEST DRAIN

K-Number: K043140 · 2004-12-08

ApplicantAtrium Medical Corp.
Decision Date2004-12-08
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EXPRESS AND OASIS CHEST DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Atrium Medical Corp.. It received FDA 510(k) clearance on 2004-12-08 under 510(k) number K043140. 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 EXPRESS AND OASIS CHEST DRAIN?

EXPRESS AND OASIS CHEST DRAIN is a medical device that received FDA 510(k) clearance on 2004-12-08. The listed applicant is Atrium Medical Corp.. The 510(k) number is K043140.

When did EXPRESS AND OASIS CHEST DRAIN receive FDA 510(k) clearance?

EXPRESS AND OASIS CHEST DRAIN received FDA 510(k) clearance on 2004-12-08, under 510(k) number K043140.

Who is the listed applicant for EXPRESS AND OASIS CHEST DRAIN?

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

What is the FDA product code for EXPRESS AND OASIS CHEST DRAIN?

The FDA product code for EXPRESS AND OASIS CHEST DRAIN is CAC.

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Other records listing Atrium Medical Corp. as applicant

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Related Devices (Code: CAC)

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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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