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FDA 510(k)

MILLER/NADLER GLARE TESTER

K-Number: K812706 · 1981-11-16

ApplicantMosebach Electric & Supply
Decision Date1981-11-16
Product CodeHOS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MILLER/NADLER GLARE TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Mosebach Electric & Supply. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K812706. The device is classified under product code HOS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLER/NADLER GLARE TESTER?

MILLER/NADLER GLARE TESTER is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Mosebach Electric & Supply. The 510(k) number is K812706.

When did MILLER/NADLER GLARE TESTER receive FDA 510(k) clearance?

MILLER/NADLER GLARE TESTER received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812706.

Who is the listed applicant for MILLER/NADLER GLARE TESTER?

The FDA 510(k) record lists Mosebach Electric & Supply as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILLER/NADLER GLARE TESTER?

The FDA product code for MILLER/NADLER GLARE TESTER is HOS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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