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FDA 510(k)

BARD MALECOT AND PEZZER DRAINS

K-Number: K070879 · 2007-04-24

Decision Date2007-04-24
Product CodeFEW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD MALECOT AND PEZZER DRAINS 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 2007-04-24 under 510(k) number K070879. The device is classified under product code FEW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD MALECOT AND PEZZER DRAINS?

BARD MALECOT AND PEZZER DRAINS is a medical device that received FDA 510(k) clearance on 2007-04-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K070879.

When did BARD MALECOT AND PEZZER DRAINS receive FDA 510(k) clearance?

BARD MALECOT AND PEZZER DRAINS received FDA 510(k) clearance on 2007-04-24, under 510(k) number K070879.

Who is the listed applicant for BARD MALECOT AND PEZZER DRAINS?

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 BARD MALECOT AND PEZZER DRAINS?

The FDA product code for BARD MALECOT AND PEZZER DRAINS is FEW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing C.R. Bard, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 616 devices →

Related Devices (Code: FEW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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