FDA 510(k)

NIAGARA SLIM-CATH

K-Number: K010778 · 2001-04-13

Decision Date2001-04-13

Product CodeMPB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

NIAGARA SLIM-CATH 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 2001-04-13 under 510(k) number K010778. The device is classified under product code MPB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIAGARA SLIM-CATH?

NIAGARA SLIM-CATH is a medical device that received FDA 510(k) clearance on 2001-04-13. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K010778.

When did NIAGARA SLIM-CATH receive FDA 510(k) clearance?

NIAGARA SLIM-CATH received FDA 510(k) clearance on 2001-04-13, under 510(k) number K010778.

Who is the listed applicant for NIAGARA SLIM-CATH?

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 NIAGARA SLIM-CATH?

The FDA product code for NIAGARA SLIM-CATH is MPB.

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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.