FDA 510(k)

SOFT-CELL DUAL LUMEN CATHETERS

K-Number: K030277 · 2003-08-06

Decision Date2003-08-06

Product CodeMSD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SOFT-CELL DUAL LUMEN CATHETERS 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 2003-08-06 under 510(k) number K030277. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOFT-CELL DUAL LUMEN CATHETERS?

SOFT-CELL DUAL LUMEN CATHETERS is a medical device that received FDA 510(k) clearance on 2003-08-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K030277.

When did SOFT-CELL DUAL LUMEN CATHETERS receive FDA 510(k) clearance?

SOFT-CELL DUAL LUMEN CATHETERS received FDA 510(k) clearance on 2003-08-06, under 510(k) number K030277.

Who is the listed applicant for SOFT-CELL DUAL LUMEN CATHETERS?

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 SOFT-CELL DUAL LUMEN CATHETERS?

The FDA product code for SOFT-CELL DUAL LUMEN CATHETERS is MSD.

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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.