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FDA 510(k)

ANOMALOSCOPE QUADRANT TEST-6

K-Number: K913962 · 1991-10-23

ApplicantLkc Technologies, Inc.
Decision Date1991-10-23
Product CodeHIW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANOMALOSCOPE QUADRANT TEST-6 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 1991-10-23 under 510(k) number K913962. The device is classified under product code HIW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANOMALOSCOPE QUADRANT TEST-6?

ANOMALOSCOPE QUADRANT TEST-6 is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K913962.

When did ANOMALOSCOPE QUADRANT TEST-6 receive FDA 510(k) clearance?

ANOMALOSCOPE QUADRANT TEST-6 received FDA 510(k) clearance on 1991-10-23, under 510(k) number K913962.

Who is the listed applicant for ANOMALOSCOPE QUADRANT TEST-6?

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 ANOMALOSCOPE QUADRANT TEST-6?

The FDA product code for ANOMALOSCOPE QUADRANT TEST-6 is HIW.

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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.

K914163SCOPTOPIC SENSITIVITY TEST-1[SST-1]K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]K874336PATTERN DISCRIMINATION PERIMETERK820414UNIVERSAL TESTING & ANALYSIS SYSTEMSK790109TELEMETRY, BIOMEDICALK760199ELECTRORETINOGRAPH

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Related Devices (Code: HIW)

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.

K930575KAMPPETER ANOMALOSCOPEBova Intl.K860174GUNKEL CHROMAGRAPH COLOR VISION TESTERChromagraphics, 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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