COOPER VISION SYSTEM VI U/S MODULE
K-Number: K853070 · 1985-08-20
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Device Summary
Frequently Asked Questions
What is the COOPER VISION SYSTEM VI U/S MODULE?
COOPER VISION SYSTEM VI U/S MODULE is a medical device that received FDA 510(k) clearance on 1985-08-20. The listed applicant is CooperVision, Inc.. The 510(k) number is K853070.
When did COOPER VISION SYSTEM VI U/S MODULE receive FDA 510(k) clearance?
COOPER VISION SYSTEM VI U/S MODULE received FDA 510(k) clearance on 1985-08-20, under 510(k) number K853070.
Who is the listed applicant for COOPER VISION SYSTEM VI U/S MODULE?
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 COOPER VISION SYSTEM VI U/S MODULE?
The FDA product code for COOPER VISION SYSTEM VI U/S MODULE 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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