CLERZ LUBRICATING & REWETTING EYE DROPS
K-Number: K830740 · 1983-06-02
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Device Summary
Frequently Asked Questions
What is the CLERZ LUBRICATING & REWETTING EYE DROPS?
CLERZ LUBRICATING & REWETTING EYE DROPS is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is CooperVision, Inc.. The 510(k) number is K830740.
When did CLERZ LUBRICATING & REWETTING EYE DROPS receive FDA 510(k) clearance?
CLERZ LUBRICATING & REWETTING EYE DROPS received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830740.
Who is the listed applicant for CLERZ LUBRICATING & REWETTING EYE DROPS?
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 CLERZ LUBRICATING & REWETTING EYE DROPS?
The FDA product code for CLERZ LUBRICATING & REWETTING EYE DROPS is HPX.
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: HPX)
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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