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FDA 510(k)

STRYKER T4 HYTREL (R) TOGAS

K-Number: K011755 · 2001-06-22

ApplicantStryker Corp.
Decision Date2001-06-22
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER T4 HYTREL (R) TOGAS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2001-06-22 under 510(k) number K011755. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER T4 HYTREL (R) TOGAS?

STRYKER T4 HYTREL (R) TOGAS is a medical device that received FDA 510(k) clearance on 2001-06-22. The listed applicant is Stryker Corp.. The 510(k) number is K011755.

When did STRYKER T4 HYTREL (R) TOGAS receive FDA 510(k) clearance?

STRYKER T4 HYTREL (R) TOGAS received FDA 510(k) clearance on 2001-06-22, under 510(k) number K011755.

Who is the listed applicant for STRYKER T4 HYTREL (R) TOGAS?

The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER T4 HYTREL (R) TOGAS?

The FDA product code for STRYKER T4 HYTREL (R) TOGAS is LYU.

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Related Devices (Code: LYU)

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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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