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FDA 510(k)

TORAY ANTHRON BYPASS TUBES

K-Number: K861116 · 1986-05-28

ApplicantToray Industries (America), Inc.
Decision Date1986-05-28
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TORAY ANTHRON BYPASS TUBES 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 1986-05-28 under 510(k) number K861116. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TORAY ANTHRON BYPASS TUBES?

TORAY ANTHRON BYPASS TUBES is a medical device that received FDA 510(k) clearance on 1986-05-28. The listed applicant is Toray Industries (America), Inc.. The 510(k) number is K861116.

When did TORAY ANTHRON BYPASS TUBES receive FDA 510(k) clearance?

TORAY ANTHRON BYPASS TUBES received FDA 510(k) clearance on 1986-05-28, under 510(k) number K861116.

Who is the listed applicant for TORAY ANTHRON BYPASS TUBES?

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 ANTHRON BYPASS TUBES?

The FDA product code for TORAY ANTHRON BYPASS TUBES is DWF.

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

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Related Devices (Code: DWF)

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.

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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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