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FDA 510(k)

DOWNING SPECTRAL ILLUMINATOR

K-Number: K833446 · 1984-03-12

ApplicantVision Health Technology
Decision Date1984-03-12
Product CodeHLX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DOWNING SPECTRAL ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Vision Health Technology. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K833446. 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 DOWNING SPECTRAL ILLUMINATOR?

DOWNING SPECTRAL ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Vision Health Technology. The 510(k) number is K833446.

When did DOWNING SPECTRAL ILLUMINATOR receive FDA 510(k) clearance?

DOWNING SPECTRAL ILLUMINATOR received FDA 510(k) clearance on 1984-03-12, under 510(k) number K833446.

Who is the listed applicant for DOWNING SPECTRAL ILLUMINATOR?

The FDA 510(k) record lists Vision Health Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOWNING SPECTRAL ILLUMINATOR?

The FDA product code for DOWNING SPECTRAL ILLUMINATOR is HLX.

Related Clinical Trials

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Other records listing Vision Health Technology 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.

K833538DOWING OPHTHALMIC CHAIR-NON/AC POWERK833539DOWING OPHTHALMIC CHAIR AC-POWERED

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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