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FDA 510(k)

NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP

K-Number: K930572 · 1993-07-23

ApplicantAmerican Hydro-Surgical Instruments, Inc.
Decision Date1993-07-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP is the device name listed in this FDA 510(k) record. The listed applicant is American Hydro-Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K930572. 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 HYDRO-DISSECTION SYSTEM II PUMP?

NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is American Hydro-Surgical Instruments, Inc.. The 510(k) number is K930572.

When did NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP receive FDA 510(k) clearance?

NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP received FDA 510(k) clearance on 1993-07-23, under 510(k) number K930572.

Who is the listed applicant for NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP?

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

What is the FDA product code for NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP?

The FDA product code for NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP is GCJ.

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Other records listing American Hydro-Surgical Instruments, Inc. as applicant

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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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