FDA 510(k)

BARD ELIMINATOR PET BALLOON DILATORS

K-Number: K033936 · 2004-01-14

Decision Date2004-01-14

Product CodeKNQ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD ELIMINATOR PET BALLOON DILATORS 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 2004-01-14 under 510(k) number K033936. The device is classified under product code KNQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ELIMINATOR PET BALLOON DILATORS?

BARD ELIMINATOR PET BALLOON DILATORS is a medical device that received FDA 510(k) clearance on 2004-01-14. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K033936.

When did BARD ELIMINATOR PET BALLOON DILATORS receive FDA 510(k) clearance?

BARD ELIMINATOR PET BALLOON DILATORS received FDA 510(k) clearance on 2004-01-14, under 510(k) number K033936.

Who is the listed applicant for BARD ELIMINATOR PET BALLOON DILATORS?

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 ELIMINATOR PET BALLOON DILATORS?

The FDA product code for BARD ELIMINATOR PET BALLOON DILATORS is KNQ.

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Related Devices (Code: KNQ)

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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.