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FDA 510(k)

CARDIOPULMONARY BYPASS

K-Number: K810820 · 1981-04-03

ApplicantDlp, Inc.
Decision Date1981-04-03
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOPULMONARY BYPASS is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1981-04-03 under 510(k) number K810820. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOPULMONARY BYPASS?

CARDIOPULMONARY BYPASS is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Dlp, Inc.. The 510(k) number is K810820.

When did CARDIOPULMONARY BYPASS receive FDA 510(k) clearance?

CARDIOPULMONARY BYPASS received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810820.

Who is the listed applicant for CARDIOPULMONARY BYPASS?

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

What is the FDA product code for CARDIOPULMONARY BYPASS?

The FDA product code for CARDIOPULMONARY BYPASS is DWF.

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Other records listing Dlp, Inc. as applicant

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Related Devices (Code: DWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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