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FDA 510(k)

WM. HARVEY PARALLEL PLATE MEMBRANE BLOOD

K-Number: K831705 · 1983-07-18

ApplicantC.R. Bard, Inc.
Decision Date1983-07-18
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WM. HARVEY PARALLEL PLATE MEMBRANE 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 1983-07-18 under 510(k) number K831705. 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 PARALLEL PLATE MEMBRANE BLOOD?

WM. HARVEY PARALLEL PLATE MEMBRANE BLOOD is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K831705.

When did WM. HARVEY PARALLEL PLATE MEMBRANE BLOOD receive FDA 510(k) clearance?

WM. HARVEY PARALLEL PLATE MEMBRANE BLOOD received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831705.

Who is the listed applicant for WM. HARVEY PARALLEL PLATE MEMBRANE 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 PARALLEL PLATE MEMBRANE BLOOD?

The FDA product code for WM. HARVEY PARALLEL PLATE MEMBRANE 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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