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FDA 510(k)

WILLIAM HARVEY FLOWMETER SYSTEM

K-Number: K810314 · 1981-02-19

ApplicantC.R. Bard, Inc.
Decision Date1981-02-19
Product CodeBYM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY FLOWMETER SYSTEM 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 1981-02-19 under 510(k) number K810314. The device is classified under product code BYM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAM HARVEY FLOWMETER SYSTEM?

WILLIAM HARVEY FLOWMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1981-02-19. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K810314.

When did WILLIAM HARVEY FLOWMETER SYSTEM receive FDA 510(k) clearance?

WILLIAM HARVEY FLOWMETER SYSTEM received FDA 510(k) clearance on 1981-02-19, under 510(k) number K810314.

Who is the listed applicant for WILLIAM HARVEY FLOWMETER SYSTEM?

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 FLOWMETER SYSTEM?

The FDA product code for WILLIAM HARVEY FLOWMETER SYSTEM is BYM.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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