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FDA 510(k)

WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD

K-Number: K821477 · 1982-11-01

ApplicantC.R. Bard, Inc.
Decision Date1982-11-01
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD 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 1982-11-01 under 510(k) number K821477. 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 WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD?

WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD is a medical device that received FDA 510(k) clearance on 1982-11-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K821477.

When did WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD receive FDA 510(k) clearance?

WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD received FDA 510(k) clearance on 1982-11-01, under 510(k) number K821477.

Who is the listed applicant for WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD?

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 WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD?

The FDA product code for WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD 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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