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FDA 510(k)

NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE

K-Number: K896118 · 1990-03-28

Decision Date1990-03-28
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE 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 1990-03-28 under 510(k) number K896118. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE?

NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is American Surgical Instruments Corp.. The 510(k) number is K896118.

When did NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE receive FDA 510(k) clearance?

NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE received FDA 510(k) clearance on 1990-03-28, under 510(k) number K896118.

Who is the listed applicant for NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE?

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 OB-GYN USE?

The FDA product code for NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE is HET.

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: HET)

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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