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FDA 510(k)

HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM

K-Number: K021813 · 2003-05-09

ApplicantHydrocision, Inc.
Decision Date2003-05-09
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hydrocision, Inc.. It received FDA 510(k) clearance on 2003-05-09 under 510(k) number K021813. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM?

HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM is a medical device that received FDA 510(k) clearance on 2003-05-09. The listed applicant is Hydrocision, Inc.. The 510(k) number is K021813.

When did HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM receive FDA 510(k) clearance?

HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM received FDA 510(k) clearance on 2003-05-09, under 510(k) number K021813.

Who is the listed applicant for HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM?

The FDA 510(k) record lists Hydrocision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM?

The FDA product code for HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM is FQH.

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Other records listing Hydrocision, Inc. as applicant

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Related Devices (Code: FQH)

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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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