MUSTANG BALLOON DILATAION CATHETERS
K-Number: K110122 · 2011-05-12
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Device Summary
Frequently Asked Questions
What is the MUSTANG BALLOON DILATAION CATHETERS?
MUSTANG BALLOON DILATAION CATHETERS is a medical device that received FDA 510(k) clearance on 2011-05-12. The listed applicant is Boston Scientific. The 510(k) number is K110122.
When did MUSTANG BALLOON DILATAION CATHETERS receive FDA 510(k) clearance?
MUSTANG BALLOON DILATAION CATHETERS received FDA 510(k) clearance on 2011-05-12, under 510(k) number K110122.
Who is the listed applicant for MUSTANG BALLOON DILATAION 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 DILATAION CATHETERS?
The FDA product code for MUSTANG BALLOON DILATAION CATHETERS is FGE.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Boston Scientific as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FGE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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