BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC
K-Number: K113267 · 2011-12-02
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Device Summary
Frequently Asked Questions
What is the BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC?
BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC is a medical device that received FDA 510(k) clearance on 2011-12-02. The listed applicant is CooperVision, Inc.. The 510(k) number is K113267.
When did BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC receive FDA 510(k) clearance?
BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC received FDA 510(k) clearance on 2011-12-02, under 510(k) number K113267.
Who is the listed applicant for BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC?
The FDA product code for BIOPMEDICS52,52 1DAY,52 TORIC,52 1DAY TORIC 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 CooperVision, 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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