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FDA 510(k)

NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES

K-Number: K913944 · 1992-03-09

ApplicantAmerican Surgical Instruments Corp.
Decision Date1992-03-09
Product CodeHET
Advisory CommitteeOB
DecisionUnknown

Device Summary

NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES 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 1992-03-09 under 510(k) number K913944. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES?

NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-03-09. The listed applicant is American Surgical Instruments Corp.. The 510(k) number is K913944.

When did NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES receive FDA 510(k) clearance?

NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES received FDA 510(k) clearance on 1992-03-09, under 510(k) number K913944.

Who is the listed applicant for NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES?

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 HYDRO DISSECTION PUMP & ACCESSORIES?

The FDA product code for NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES is HET.

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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.

K921716DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEMK921457IRRIGATION PUMPS AND TUBING AND SUCTION TUBINGK913999NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBEK911274UNIPOLAR COAGULATOR PROBE SYSTEMK896118NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE

Related Devices (Code: HET)

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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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