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FDA 510(k)

CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS

K-Number: K992950 · 1999-11-18

Decision Date1999-11-18
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Prosthetic Soft Lens Corp.. It received FDA 510(k) clearance on 1999-11-18 under 510(k) number K992950. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS?

CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS is a medical device that received FDA 510(k) clearance on 1999-11-18. The listed applicant is Prosthetic Soft Lens Corp.. The 510(k) number is K992950.

When did CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS receive FDA 510(k) clearance?

CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS received FDA 510(k) clearance on 1999-11-18, under 510(k) number K992950.

Who is the listed applicant for CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS?

The FDA 510(k) record lists Prosthetic Soft Lens Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS?

The FDA product code for CUSTOM PROSTHETIC (HEFILCON A) SOFT LENS is LPL.

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.

Related Devices (Code: LPL)

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

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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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