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FDA 510(k)

ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES

K-Number: K042242 · 2004-09-15

Decision Date2004-09-15
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Alden Optical Labs., Inc.. It received FDA 510(k) clearance on 2004-09-15 under 510(k) number K042242. 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 ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES?

ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES is a medical device that received FDA 510(k) clearance on 2004-09-15. The listed applicant is Alden Optical Labs., Inc.. The 510(k) number is K042242.

When did ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES receive FDA 510(k) clearance?

ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES received FDA 510(k) clearance on 2004-09-15, under 510(k) number K042242.

Who is the listed applicant for ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES?

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

What is the FDA product code for ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES?

The FDA product code for ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES 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.

Other records listing Alden Optical Labs., Inc. 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 10 devices →

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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