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FDA 510(k)

STRYKER IRRIGATION TUBE SET

K-Number: K000493 · 2000-05-15

Decision Date2000-05-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER IRRIGATION TUBE SET is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2000-05-15 under 510(k) number K000493. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER IRRIGATION TUBE SET?

STRYKER IRRIGATION TUBE SET is a medical device that received FDA 510(k) clearance on 2000-05-15. The listed applicant is Stryker Endoscopy. The 510(k) number is K000493.

When did STRYKER IRRIGATION TUBE SET receive FDA 510(k) clearance?

STRYKER IRRIGATION TUBE SET received FDA 510(k) clearance on 2000-05-15, under 510(k) number K000493.

Who is the listed applicant for STRYKER IRRIGATION TUBE SET?

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

What is the FDA product code for STRYKER IRRIGATION TUBE SET?

The FDA product code for STRYKER IRRIGATION TUBE SET is GCJ.

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 Stryker Endoscopy 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.

View all 97 devices →

Related Devices (Code: GCJ)

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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