LENSINE EXTRA STRENGTH CLEANER
K-Number: K812433 · 1981-09-21
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Device Summary
Frequently Asked Questions
What is the LENSINE EXTRA STRENGTH CLEANER?
LENSINE EXTRA STRENGTH CLEANER is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is CooperVision, Inc.. The 510(k) number is K812433.
When did LENSINE EXTRA STRENGTH CLEANER receive FDA 510(k) clearance?
LENSINE EXTRA STRENGTH CLEANER received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812433.
Who is the listed applicant for LENSINE EXTRA STRENGTH CLEANER?
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 LENSINE EXTRA STRENGTH CLEANER?
The FDA product code for LENSINE EXTRA STRENGTH CLEANER 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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