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FDA 510(k)

TORAY VASCULAR PROSTHESIS

K-Number: K884083 · 1989-01-12

ApplicantToray Industries (America), Inc.
Decision Date1989-01-12
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TORAY VASCULAR PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Toray Industries (America), Inc.. It received FDA 510(k) clearance on 1989-01-12 under 510(k) number K884083. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TORAY VASCULAR PROSTHESIS?

TORAY VASCULAR PROSTHESIS is a medical device that received FDA 510(k) clearance on 1989-01-12. The listed applicant is Toray Industries (America), Inc.. The 510(k) number is K884083.

When did TORAY VASCULAR PROSTHESIS receive FDA 510(k) clearance?

TORAY VASCULAR PROSTHESIS received FDA 510(k) clearance on 1989-01-12, under 510(k) number K884083.

Who is the listed applicant for TORAY VASCULAR PROSTHESIS?

The FDA 510(k) record lists Toray Industries (America), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TORAY VASCULAR PROSTHESIS?

The FDA product code for TORAY VASCULAR PROSTHESIS is DSY.

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Other records listing Toray Industries (America), Inc. as applicant

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Related Devices (Code: DSY)

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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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