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FDA 510(k)

MUSTANG BALLOON DILATATION CATHETERS

K-Number: K103751 · 2011-03-22

ApplicantBoston Scientific
Decision Date2011-03-22
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MUSTANG BALLOON DILATATION CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific. It received FDA 510(k) clearance on 2011-03-22 under 510(k) number K103751. 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 MUSTANG BALLOON DILATATION CATHETERS?

MUSTANG BALLOON DILATATION CATHETERS is a medical device that received FDA 510(k) clearance on 2011-03-22. The listed applicant is Boston Scientific. The 510(k) number is K103751.

When did MUSTANG BALLOON DILATATION CATHETERS receive FDA 510(k) clearance?

MUSTANG BALLOON DILATATION CATHETERS received FDA 510(k) clearance on 2011-03-22, under 510(k) number K103751.

Who is the listed applicant for MUSTANG BALLOON DILATATION CATHETERS?

The FDA 510(k) record lists Boston Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUSTANG BALLOON DILATATION CATHETERS?

The FDA product code for MUSTANG BALLOON DILATATION CATHETERS 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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