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FDA 510(k)

CANON IOL ESTIMATOR KU-1

K-Number: K881889 · 1988-09-15

ApplicantCanon USA, Inc.
Decision Date1988-09-15
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CANON IOL ESTIMATOR KU-1 is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1988-09-15 under 510(k) number K881889. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON IOL ESTIMATOR KU-1?

CANON IOL ESTIMATOR KU-1 is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is Canon USA, Inc.. The 510(k) number is K881889.

When did CANON IOL ESTIMATOR KU-1 receive FDA 510(k) clearance?

CANON IOL ESTIMATOR KU-1 received FDA 510(k) clearance on 1988-09-15, under 510(k) number K881889.

Who is the listed applicant for CANON IOL ESTIMATOR KU-1?

The FDA 510(k) record lists Canon USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANON IOL ESTIMATOR KU-1?

The FDA product code for CANON IOL ESTIMATOR KU-1 is IYO.

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Other records listing Canon USA, Inc. as applicant

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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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