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FDA 510(k)

WILLIAM HARVEY H-1700 ADULT BLOOD OXYG-

K-Number: K831122 · 1983-05-25

ApplicantC.R. Bard, Inc.
Decision Date1983-05-25
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY H-1700 ADULT BLOOD OXYG- 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 1983-05-25 under 510(k) number K831122. 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 H-1700 ADULT BLOOD OXYG-?

WILLIAM HARVEY H-1700 ADULT BLOOD OXYG- is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K831122.

When did WILLIAM HARVEY H-1700 ADULT BLOOD OXYG- receive FDA 510(k) clearance?

WILLIAM HARVEY H-1700 ADULT BLOOD OXYG- received FDA 510(k) clearance on 1983-05-25, under 510(k) number K831122.

Who is the listed applicant for WILLIAM HARVEY H-1700 ADULT BLOOD OXYG-?

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 H-1700 ADULT BLOOD OXYG-?

The FDA product code for WILLIAM HARVEY H-1700 ADULT BLOOD OXYG- 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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