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FDA 510(k)

PARAGON LENS CARRIER

K-Number: K993486 · 1999-12-22

Decision Date1999-12-22
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PARAGON LENS CARRIER 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 1999-12-22 under 510(k) number K993486. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAGON LENS CARRIER?

PARAGON LENS CARRIER is a medical device that received FDA 510(k) clearance on 1999-12-22. The listed applicant is Paragon Vision Sciences. The 510(k) number is K993486.

When did PARAGON LENS CARRIER receive FDA 510(k) clearance?

PARAGON LENS CARRIER received FDA 510(k) clearance on 1999-12-22, under 510(k) number K993486.

Who is the listed applicant for PARAGON LENS CARRIER?

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 PARAGON LENS CARRIER?

The FDA product code for PARAGON LENS CARRIER is LRX.

Related Clinical Trials

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.

Other records listing Paragon Vision Sciences as applicant

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.

View all 15 devices →

Related Devices (Code: LRX)

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.

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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