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FDA 510(k)

ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY

K-Number: K060745 · 2006-06-23

ApplicantAsahi Intecc Co., Ltd.
Decision Date2006-06-23
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2006-06-23 under 510(k) number K060745. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY?

ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY is a medical device that received FDA 510(k) clearance on 2006-06-23. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K060745.

When did ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY receive FDA 510(k) clearance?

ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY received FDA 510(k) clearance on 2006-06-23, under 510(k) number K060745.

Who is the listed applicant for ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY?

The FDA 510(k) record lists Asahi Intecc Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY?

The FDA product code for ASAHI TORNUS SUPPORT CATHETER WITH TORQUE DEVICE ACCESSORY is DQY.

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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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