IMAGER TORQUE CATHETER
K-Number: K965229 · 1997-03-04
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Device Summary
Frequently Asked Questions
What is the IMAGER TORQUE CATHETER?
IMAGER TORQUE CATHETER is a medical device that received FDA 510(k) clearance on 1997-03-04. The listed applicant is Boston Scientific Corp. The 510(k) number is K965229.
When did IMAGER TORQUE CATHETER receive FDA 510(k) clearance?
IMAGER TORQUE CATHETER received FDA 510(k) clearance on 1997-03-04, under 510(k) number K965229.
Who is the listed applicant for IMAGER TORQUE CATHETER?
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 IMAGER TORQUE CATHETER?
The FDA product code for IMAGER TORQUE CATHETER is KOD.
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 Corp 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: KOD)
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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