FDA 510(k)

BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM

K-Number: K031295 · 2003-05-15

Decision Date2003-05-15

Product CodePAG

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BARD INNERLACE BIOURETHRAL SUPPORT 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 2003-05-15 under 510(k) number K031295. The device is classified under product code PAG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM?

BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-05-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K031295.

When did BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM receive FDA 510(k) clearance?

BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM received FDA 510(k) clearance on 2003-05-15, under 510(k) number K031295.

Who is the listed applicant for BARD INNERLACE BIOURETHRAL SUPPORT 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 BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM?

The FDA product code for BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM is PAG.

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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.