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FDA 510(k)

BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV

K-Number: K913915 · 1992-01-21

ApplicantBard Cardiosurgery Div
Decision Date1992-01-21
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV is the device name listed in this FDA 510(k) record. The listed applicant is Bard Cardiosurgery Div. It received FDA 510(k) clearance on 1992-01-21 under 510(k) number K913915. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV?

BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV is a medical device that received FDA 510(k) clearance on 1992-01-21. The listed applicant is Bard Cardiosurgery Div. The 510(k) number is K913915.

When did BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV receive FDA 510(k) clearance?

BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV received FDA 510(k) clearance on 1992-01-21, under 510(k) number K913915.

Who is the listed applicant for BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV?

The FDA 510(k) record lists Bard Cardiosurgery Div as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV?

The FDA product code for BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV is DTN.

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Other records listing Bard Cardiosurgery Div as applicant

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Related Devices (Code: DTN)

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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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