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FDA 510(k)

OPTIONAL PROBE OF CANON IOL ESTIMATOR KU-1

K-Number: K891225 · 1989-05-31

ApplicantCanon USA, Inc.
Decision Date1989-05-31
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OPTIONAL PROBE OF 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 1989-05-31 under 510(k) number K891225. 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 OPTIONAL PROBE OF CANON IOL ESTIMATOR KU-1?

OPTIONAL PROBE OF CANON IOL ESTIMATOR KU-1 is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is Canon USA, Inc.. The 510(k) number is K891225.

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

OPTIONAL PROBE OF CANON IOL ESTIMATOR KU-1 received FDA 510(k) clearance on 1989-05-31, under 510(k) number K891225.

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

The FDA product code for OPTIONAL PROBE OF 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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