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FDA 510(k)

SUBJECTIVE REFRACTOR, MOSEL SR-111

K-Number: K771914 · 1977-11-09

ApplicantAmerican Optical Corp.
Decision Date1977-11-09
Product CodeHKO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUBJECTIVE REFRACTOR, MOSEL SR-111 is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1977-11-09 under 510(k) number K771914. The device is classified under product code HKO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUBJECTIVE REFRACTOR, MOSEL SR-111?

SUBJECTIVE REFRACTOR, MOSEL SR-111 is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is American Optical Corp.. The 510(k) number is K771914.

When did SUBJECTIVE REFRACTOR, MOSEL SR-111 receive FDA 510(k) clearance?

SUBJECTIVE REFRACTOR, MOSEL SR-111 received FDA 510(k) clearance on 1977-11-09, under 510(k) number K771914.

Who is the listed applicant for SUBJECTIVE REFRACTOR, MOSEL SR-111?

The FDA 510(k) record lists American Optical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUBJECTIVE REFRACTOR, MOSEL SR-111?

The FDA product code for SUBJECTIVE REFRACTOR, MOSEL SR-111 is HKO.

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Related Devices (Code: HKO)

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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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