ALDEN HP (HIOXIFILCON B) SPHERE & TORIC SOFT CONTACT LENSES
K-Number: K042242 · 2004-09-15
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Device Summary
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.
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
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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