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FDA 510(k)

CORSON AND NEZHAT SUCTION/IRRIGATION PROBES

K-Number: K935786 · 1994-05-19

Decision Date1994-05-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORSON AND NEZHAT SUCTION/IRRIGATION PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1994-05-19 under 510(k) number K935786. 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 CORSON AND NEZHAT SUCTION/IRRIGATION PROBES?

CORSON AND NEZHAT SUCTION/IRRIGATION PROBES is a medical device that received FDA 510(k) clearance on 1994-05-19. The listed applicant is Cabot Medical Corp.. The 510(k) number is K935786.

When did CORSON AND NEZHAT SUCTION/IRRIGATION PROBES receive FDA 510(k) clearance?

CORSON AND NEZHAT SUCTION/IRRIGATION PROBES received FDA 510(k) clearance on 1994-05-19, under 510(k) number K935786.

Who is the listed applicant for CORSON AND NEZHAT SUCTION/IRRIGATION PROBES?

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

What is the FDA product code for CORSON AND NEZHAT SUCTION/IRRIGATION PROBES?

The FDA product code for CORSON AND NEZHAT SUCTION/IRRIGATION PROBES 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 Cabot Medical Corp. 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.

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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

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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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