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FDA 510(k)

WM. HARVEY OVERPRESSURE SAFETY VALVE

K-Number: K820297 · 1982-03-12

ApplicantC.R. Bard, Inc.
Decision Date1982-03-12
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WM. HARVEY OVERPRESSURE SAFETY VALVE 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 1982-03-12 under 510(k) number K820297. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WM. HARVEY OVERPRESSURE SAFETY VALVE?

WM. HARVEY OVERPRESSURE SAFETY VALVE is a medical device that received FDA 510(k) clearance on 1982-03-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K820297.

When did WM. HARVEY OVERPRESSURE SAFETY VALVE receive FDA 510(k) clearance?

WM. HARVEY OVERPRESSURE SAFETY VALVE received FDA 510(k) clearance on 1982-03-12, under 510(k) number K820297.

Who is the listed applicant for WM. HARVEY OVERPRESSURE SAFETY VALVE?

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 OVERPRESSURE SAFETY VALVE?

The FDA product code for WM. HARVEY OVERPRESSURE SAFETY VALVE is DTL.

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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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