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FDA 510(k)

COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY

K-Number: K893402 · 1989-06-23

ApplicantAtrium Medical Corp.
Decision Date1989-06-23
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY 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 1989-06-23 under 510(k) number K893402. 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 COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY?

COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Atrium Medical Corp.. The 510(k) number is K893402.

When did COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY receive FDA 510(k) clearance?

COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY received FDA 510(k) clearance on 1989-06-23, under 510(k) number K893402.

Who is the listed applicant for COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY?

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 COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY?

The FDA product code for COMPACT 2052(TM) DUAL COLLECTION BLOOD RECOVERY is CAC.

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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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