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FDA 510(k)

SCOPTOPIC SENSITIVITY TEST-1[SST-1]

K-Number: K914163 · 1991-10-25

ApplicantLkc Technologies, Inc.
Decision Date1991-10-25
Product CodeHLX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SCOPTOPIC SENSITIVITY TEST-1[SST-1] is the device name listed in this FDA 510(k) record. The listed applicant is Lkc Technologies, Inc.. It received FDA 510(k) clearance on 1991-10-25 under 510(k) number K914163. 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 SCOPTOPIC SENSITIVITY TEST-1[SST-1]?

SCOPTOPIC SENSITIVITY TEST-1[SST-1] is a medical device that received FDA 510(k) clearance on 1991-10-25. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K914163.

When did SCOPTOPIC SENSITIVITY TEST-1[SST-1] receive FDA 510(k) clearance?

SCOPTOPIC SENSITIVITY TEST-1[SST-1] received FDA 510(k) clearance on 1991-10-25, under 510(k) number K914163.

Who is the listed applicant for SCOPTOPIC SENSITIVITY TEST-1[SST-1]?

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

What is the FDA product code for SCOPTOPIC SENSITIVITY TEST-1[SST-1]?

The FDA product code for SCOPTOPIC SENSITIVITY TEST-1[SST-1] is HLX.

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Other records listing Lkc Technologies, 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.

K913962ANOMALOSCOPE QUADRANT TEST-6K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]K874336PATTERN DISCRIMINATION PERIMETERK820414UNIVERSAL TESTING & ANALYSIS SYSTEMSK790109TELEMETRY, BIOMEDICALK760199ELECTRORETINOGRAPH

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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 TesterK873990IRAS EDS INTERFEROMETRIC STIMULATORRandwal Instrument Co., Inc.K853812PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)Biosan Laboratories, 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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