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FDA 510(k)

NYX GOLF VISION SYSTEM

K-Number: K953245 · 1995-07-19

ApplicantNyx Golf, Inc.
Decision Date1995-07-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NYX GOLF VISION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nyx Golf, Inc.. It received FDA 510(k) clearance on 1995-07-19 under 510(k) number K953245. 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 NYX GOLF VISION SYSTEM?

NYX GOLF VISION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-19. The listed applicant is Nyx Golf, Inc.. The 510(k) number is K953245.

When did NYX GOLF VISION SYSTEM receive FDA 510(k) clearance?

NYX GOLF VISION SYSTEM received FDA 510(k) clearance on 1995-07-19, under 510(k) number K953245.

Who is the listed applicant for NYX GOLF VISION SYSTEM?

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

What is the FDA product code for NYX GOLF VISION SYSTEM?

The FDA product code for NYX GOLF VISION SYSTEM is HQY.

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Related Devices (Code: HQY)

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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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