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FDA 510(k)

EVACUATION KIT #7-510-14

K-Number: K914861 · 1992-01-27

ApplicantNorthgate Technologies, Inc.
Decision Date1992-01-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EVACUATION KIT #7-510-14 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 1992-01-27 under 510(k) number K914861. 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 EVACUATION KIT #7-510-14?

EVACUATION KIT #7-510-14 is a medical device that received FDA 510(k) clearance on 1992-01-27. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K914861.

When did EVACUATION KIT #7-510-14 receive FDA 510(k) clearance?

EVACUATION KIT #7-510-14 received FDA 510(k) clearance on 1992-01-27, under 510(k) number K914861.

Who is the listed applicant for EVACUATION KIT #7-510-14?

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 EVACUATION KIT #7-510-14?

The FDA product code for EVACUATION KIT #7-510-14 is GCJ.

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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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