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FDA 510(k)

SUCTION/IRRIGATION Y TUBING SET

K-Number: K922655 · 1992-07-14

Decision Date1992-07-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION/IRRIGATION Y TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Core Dynamics, Inc.. It received FDA 510(k) clearance on 1992-07-14 under 510(k) number K922655. 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 SUCTION/IRRIGATION Y TUBING SET?

SUCTION/IRRIGATION Y TUBING SET is a medical device that received FDA 510(k) clearance on 1992-07-14. The listed applicant is Core Dynamics, Inc.. The 510(k) number is K922655.

When did SUCTION/IRRIGATION Y TUBING SET receive FDA 510(k) clearance?

SUCTION/IRRIGATION Y TUBING SET received FDA 510(k) clearance on 1992-07-14, under 510(k) number K922655.

Who is the listed applicant for SUCTION/IRRIGATION Y TUBING SET?

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

What is the FDA product code for SUCTION/IRRIGATION Y TUBING SET?

The FDA product code for SUCTION/IRRIGATION Y TUBING 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 Core Dynamics, Inc. 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 23 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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