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FDA 510(k)

USCI MULLINS TRANSSEPTAL CATHETER INTRO.

K-Number: K791963 · 1979-11-13

ApplicantC.R. Bard, Inc.
Decision Date1979-11-13
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI MULLINS TRANSSEPTAL CATHETER INTRO. 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 1979-11-13 under 510(k) number K791963. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI MULLINS TRANSSEPTAL CATHETER INTRO.?

USCI MULLINS TRANSSEPTAL CATHETER INTRO. is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K791963.

When did USCI MULLINS TRANSSEPTAL CATHETER INTRO. receive FDA 510(k) clearance?

USCI MULLINS TRANSSEPTAL CATHETER INTRO. received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791963.

Who is the listed applicant for USCI MULLINS TRANSSEPTAL CATHETER INTRO.?

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 USCI MULLINS TRANSSEPTAL CATHETER INTRO.?

The FDA product code for USCI MULLINS TRANSSEPTAL CATHETER INTRO. is DYB.

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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.

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