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FDA 510(k)

SERIES TEN THOUSAND OCUTOME

K-Number: K871871 · 1987-06-11

ApplicantCooperVision, Inc.
Decision Date1987-06-11
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SERIES TEN THOUSAND OCUTOME is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1987-06-11 under 510(k) number K871871. 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 SERIES TEN THOUSAND OCUTOME?

SERIES TEN THOUSAND OCUTOME is a medical device that received FDA 510(k) clearance on 1987-06-11. The listed applicant is CooperVision, Inc.. The 510(k) number is K871871.

When did SERIES TEN THOUSAND OCUTOME receive FDA 510(k) clearance?

SERIES TEN THOUSAND OCUTOME received FDA 510(k) clearance on 1987-06-11, under 510(k) number K871871.

Who is the listed applicant for SERIES TEN THOUSAND OCUTOME?

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 SERIES TEN THOUSAND OCUTOME?

The FDA product code for SERIES TEN THOUSAND OCUTOME 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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