Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
PMA Number: P950020 · 2026-01-27
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Device Summary
Frequently Asked Questions
What is the Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring?
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring is a medical device that received FDA 510(k) clearance on 2026-01-27. The listed applicant is Boston Scientific Corp.
When did Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring receive FDA 510(k) clearance?
The clearance date for Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring can be found in the official FDA records.
Who is the listed applicant for Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring?
The FDA product code for Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring is NWX.
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.
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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