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FDA 510(k)

KOI(TM) INSTRUMENT TRAYS

K-Number: K881095 · 1988-04-06

ApplicantCooperVision, Inc.
Decision Date1988-04-06
Product CodeLRP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KOI(TM) INSTRUMENT TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1988-04-06 under 510(k) number K881095. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOI(TM) INSTRUMENT TRAYS?

KOI(TM) INSTRUMENT TRAYS is a medical device that received FDA 510(k) clearance on 1988-04-06. The listed applicant is CooperVision, Inc.. The 510(k) number is K881095.

When did KOI(TM) INSTRUMENT TRAYS receive FDA 510(k) clearance?

KOI(TM) INSTRUMENT TRAYS received FDA 510(k) clearance on 1988-04-06, under 510(k) number K881095.

Who is the listed applicant for KOI(TM) INSTRUMENT TRAYS?

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 KOI(TM) INSTRUMENT TRAYS?

The FDA product code for KOI(TM) INSTRUMENT TRAYS is LRP.

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Related Devices (Code: LRP)

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.

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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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