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FDA 510(k)

HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00

K-Number: K993778 · 2000-01-06

ApplicantNorthgate Technologies, Inc.
Decision Date2000-01-06
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00 is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 2000-01-06 under 510(k) number K993778. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00?

HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00 is a medical device that received FDA 510(k) clearance on 2000-01-06. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K993778.

When did HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00 receive FDA 510(k) clearance?

HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00 received FDA 510(k) clearance on 2000-01-06, under 510(k) number K993778.

Who is the listed applicant for HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00?

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

What is the FDA product code for HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00?

The FDA product code for HYDROTOWER MANAGEMENT SYSTEM, MODEL 4-750-00 is OCX.

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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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