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FDA 510(k)

CARDIOPLEGIA RESERVOIR CAS-2000

K-Number: K841938 · 1984-08-03

ApplicantAmerican Bentley
Decision Date1984-08-03
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOPLEGIA RESERVOIR CAS-2000 is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K841938. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOPLEGIA RESERVOIR CAS-2000?

CARDIOPLEGIA RESERVOIR CAS-2000 is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is American Bentley. The 510(k) number is K841938.

When did CARDIOPLEGIA RESERVOIR CAS-2000 receive FDA 510(k) clearance?

CARDIOPLEGIA RESERVOIR CAS-2000 received FDA 510(k) clearance on 1984-08-03, under 510(k) number K841938.

Who is the listed applicant for CARDIOPLEGIA RESERVOIR CAS-2000?

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

What is the FDA product code for CARDIOPLEGIA RESERVOIR CAS-2000?

The FDA product code for CARDIOPLEGIA RESERVOIR CAS-2000 is DTN.

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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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