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FDA 510(k)

HURRICANE

K-Number: K952258 · 1995-07-31

ApplicantHurricane Hardware, Inc.
Decision Date1995-07-31
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HURRICANE is the device name listed in this FDA 510(k) record. The listed applicant is Hurricane Hardware, Inc.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K952258. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HURRICANE?

HURRICANE is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Hurricane Hardware, Inc.. The 510(k) number is K952258.

When did HURRICANE receive FDA 510(k) clearance?

HURRICANE received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952258.

Who is the listed applicant for HURRICANE?

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

What is the FDA product code for HURRICANE?

The FDA product code for HURRICANE is HQY.

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Related Devices (Code: HQY)

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.

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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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