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FDA 510(k)

WILLIAM HARVEY HYBID OXYGENATOR H-1700

K-Number: K853080 · 1985-10-11

ApplicantC.R. Bard, Inc.
Decision Date1985-10-11
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY HYBID OXYGENATOR H-1700 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1985-10-11 under 510(k) number K853080. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAM HARVEY HYBID OXYGENATOR H-1700?

WILLIAM HARVEY HYBID OXYGENATOR H-1700 is a medical device that received FDA 510(k) clearance on 1985-10-11. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K853080.

When did WILLIAM HARVEY HYBID OXYGENATOR H-1700 receive FDA 510(k) clearance?

WILLIAM HARVEY HYBID OXYGENATOR H-1700 received FDA 510(k) clearance on 1985-10-11, under 510(k) number K853080.

Who is the listed applicant for WILLIAM HARVEY HYBID OXYGENATOR H-1700?

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

What is the FDA product code for WILLIAM HARVEY HYBID OXYGENATOR H-1700?

The FDA product code for WILLIAM HARVEY HYBID OXYGENATOR H-1700 is DTZ.

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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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