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FDA 510(k)

BARD(R) TIP DEFLECTING ELECTRODE CATHETER

K-Number: K891908 · 1989-06-05

ApplicantC.R. Bard, Inc.
Decision Date1989-06-05
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD(R) TIP DEFLECTING ELECTRODE CATHETER 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 1989-06-05 under 510(k) number K891908. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD(R) TIP DEFLECTING ELECTRODE CATHETER?

BARD(R) TIP DEFLECTING ELECTRODE CATHETER is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K891908.

When did BARD(R) TIP DEFLECTING ELECTRODE CATHETER receive FDA 510(k) clearance?

BARD(R) TIP DEFLECTING ELECTRODE CATHETER received FDA 510(k) clearance on 1989-06-05, under 510(k) number K891908.

Who is the listed applicant for BARD(R) TIP DEFLECTING ELECTRODE CATHETER?

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(R) TIP DEFLECTING ELECTRODE CATHETER?

The FDA product code for BARD(R) TIP DEFLECTING ELECTRODE CATHETER is DRF.

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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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