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FDA 510(k)

COOPER VISION I/A SYSTEM III MODEL 1500

K-Number: K822220 · 1982-10-06

ApplicantCooperVision, Inc.
Decision Date1982-10-06
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

COOPER VISION I/A SYSTEM III MODEL 1500 is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1982-10-06 under 510(k) number K822220. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOPER VISION I/A SYSTEM III MODEL 1500?

COOPER VISION I/A SYSTEM III MODEL 1500 is a medical device that received FDA 510(k) clearance on 1982-10-06. The listed applicant is CooperVision, Inc.. The 510(k) number is K822220.

When did COOPER VISION I/A SYSTEM III MODEL 1500 receive FDA 510(k) clearance?

COOPER VISION I/A SYSTEM III MODEL 1500 received FDA 510(k) clearance on 1982-10-06, under 510(k) number K822220.

Who is the listed applicant for COOPER VISION I/A SYSTEM III MODEL 1500?

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 I/A SYSTEM III MODEL 1500?

The FDA product code for COOPER VISION I/A SYSTEM III MODEL 1500 is HQE.

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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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