COOPERVISION SYSTEM VI
K-Number: K842945 · 1984-12-11
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Device Summary
Frequently Asked Questions
What is the COOPERVISION SYSTEM VI?
COOPERVISION SYSTEM VI is a medical device that received FDA 510(k) clearance on 1984-12-11. The listed applicant is CooperVision, Inc.. The 510(k) number is K842945.
When did COOPERVISION SYSTEM VI receive FDA 510(k) clearance?
COOPERVISION SYSTEM VI received FDA 510(k) clearance on 1984-12-11, under 510(k) number K842945.
Who is the listed applicant for COOPERVISION SYSTEM VI?
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 COOPERVISION SYSTEM VI?
The FDA product code for COOPERVISION SYSTEM VI is HQC.
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: HQC)
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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