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FDA 510(k)

TAHOE SUCTION IRRIGATOR

K-Number: K911238 · 1992-11-27

Decision Date1992-11-27
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAHOE SUCTION IRRIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Tahoe Pro Instruments. It received FDA 510(k) clearance on 1992-11-27 under 510(k) number K911238. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAHOE SUCTION IRRIGATOR?

TAHOE SUCTION IRRIGATOR is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Tahoe Pro Instruments. The 510(k) number is K911238.

When did TAHOE SUCTION IRRIGATOR receive FDA 510(k) clearance?

TAHOE SUCTION IRRIGATOR received FDA 510(k) clearance on 1992-11-27, under 510(k) number K911238.

Who is the listed applicant for TAHOE SUCTION IRRIGATOR?

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

What is the FDA product code for TAHOE SUCTION IRRIGATOR?

The FDA product code for TAHOE SUCTION IRRIGATOR is GCX.

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.

Related Devices (Code: GCX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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