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FDA 510(k)

BAYLOW VISUAL ACUITY TESTER

K-Number: K781452 · 1978-10-24

ApplicantCodman & Shurtleff, Inc.
Decision Date1978-10-24
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BAYLOW VISUAL ACUITY TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1978-10-24 under 510(k) number K781452. 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 BAYLOW VISUAL ACUITY TESTER?

BAYLOW VISUAL ACUITY TESTER is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K781452.

When did BAYLOW VISUAL ACUITY TESTER receive FDA 510(k) clearance?

BAYLOW VISUAL ACUITY TESTER received FDA 510(k) clearance on 1978-10-24, under 510(k) number K781452.

Who is the listed applicant for BAYLOW VISUAL ACUITY TESTER?

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

What is the FDA product code for BAYLOW VISUAL ACUITY TESTER?

The FDA product code for BAYLOW VISUAL ACUITY TESTER is HOX.

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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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