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FDA 510(k)

NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE

K-Number: K913999 · 1991-11-01

Decision Date1991-11-01
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE is the device name listed in this FDA 510(k) record. The listed applicant is American Surgical Instruments Corp.. It received FDA 510(k) clearance on 1991-11-01 under 510(k) number K913999. 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 NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE?

NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is American Surgical Instruments Corp.. The 510(k) number is K913999.

When did NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE receive FDA 510(k) clearance?

NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE received FDA 510(k) clearance on 1991-11-01, under 510(k) number K913999.

Who is the listed applicant for NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE?

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

What is the FDA product code for NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE?

The FDA product code for NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE 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 American Surgical Instruments 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.

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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