FDA 510(k)

SPORTSIGHT GP

K-Number: K993586 · 2000-05-22

Decision Date2000-05-22

Product CodeHQD

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SPORTSIGHT GP is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Vision Sciences. It received FDA 510(k) clearance on 2000-05-22 under 510(k) number K993586. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPORTSIGHT GP?

SPORTSIGHT GP is a medical device that received FDA 510(k) clearance on 2000-05-22. The listed applicant is Paragon Vision Sciences. The 510(k) number is K993586.

When did SPORTSIGHT GP receive FDA 510(k) clearance?

SPORTSIGHT GP received FDA 510(k) clearance on 2000-05-22, under 510(k) number K993586.

Who is the listed applicant for SPORTSIGHT GP?

The FDA 510(k) record lists Paragon Vision Sciences as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPORTSIGHT GP?

The FDA product code for SPORTSIGHT GP is HQD.

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Other records listing Paragon Vision Sciences as applicant

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Related Devices (Code: HQD)

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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.