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FDA 510(k)

MILLER/NADLER GLARE TESTER

K-Number: K832762 · 1983-09-29

ApplicantTitmus Optical, Inc.
Decision Date1983-09-29
Product CodeHLX
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 Titmus Optical, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832762. The device is classified under product code HLX. 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 1983-09-29. The listed applicant is Titmus Optical, Inc.. The 510(k) number is K832762.

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

MILLER/NADLER GLARE TESTER received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832762.

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

The FDA 510(k) record lists Titmus Optical, Inc. 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 HLX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Titmus Optical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K844694TITMUS VISION TESTER IIK843096CRISTY/COTE

Related Devices (Code: HLX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K003442MODIFICATION TO EDI VERIS SYSTEMElectro-Diagnostic Imaging, Inc.K983983EDI VERIS SYSTEMElectro-Diagnostic Imaging, Inc.K925741CLARUS ENDOSCOPIC HOOK KNIFEClarus Medical Systems, Inc.K914393RETINA TESTERRetina TesterK914163SCOPTOPIC SENSITIVITY TEST-1[SST-1]Lkc Technologies, Inc.K873990IRAS EDS INTERFEROMETRIC STIMULATORRandwal Instrument Co., Inc.

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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