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FDA 510(k)

CANON AUTO ACUITOMETER CV-10

K-Number: K861416 · 1986-05-14

ApplicantCanon USA, Inc.
Decision Date1986-05-14
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CANON AUTO ACUITOMETER CV-10 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 1986-05-14 under 510(k) number K861416. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON AUTO ACUITOMETER CV-10?

CANON AUTO ACUITOMETER CV-10 is a medical device that received FDA 510(k) clearance on 1986-05-14. The listed applicant is Canon USA, Inc.. The 510(k) number is K861416.

When did CANON AUTO ACUITOMETER CV-10 receive FDA 510(k) clearance?

CANON AUTO ACUITOMETER CV-10 received FDA 510(k) clearance on 1986-05-14, under 510(k) number K861416.

Who is the listed applicant for CANON AUTO ACUITOMETER CV-10?

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 AUTO ACUITOMETER CV-10?

The FDA product code for CANON AUTO ACUITOMETER CV-10 is HOX.

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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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