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FDA 510(k)

BARD PERIPHERAL BALLOON DILATATION CATHETER

K-Number: K910822 · 1991-08-29

ApplicantC.R. Bard, Inc.
Decision Date1991-08-29
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD PERIPHERAL BALLOON DILATATION 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 1991-08-29 under 510(k) number K910822. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD PERIPHERAL BALLOON DILATATION CATHETER?

BARD PERIPHERAL BALLOON DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 1991-08-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K910822.

When did BARD PERIPHERAL BALLOON DILATATION CATHETER receive FDA 510(k) clearance?

BARD PERIPHERAL BALLOON DILATATION CATHETER received FDA 510(k) clearance on 1991-08-29, under 510(k) number K910822.

Who is the listed applicant for BARD PERIPHERAL BALLOON DILATATION 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 PERIPHERAL BALLOON DILATATION CATHETER?

The FDA product code for BARD PERIPHERAL BALLOON DILATATION CATHETER is LIT.

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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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