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FDA 510(k)

ANOMALOSCOPE PLATE TEST - 5 [APT-5]

K-Number: K875026 · 1988-02-05

ApplicantLkc Technologies, Inc.
Decision Date1988-02-05
Product CodeHIT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANOMALOSCOPE PLATE TEST - 5 [APT-5] 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 1988-02-05 under 510(k) number K875026. The device is classified under product code HIT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANOMALOSCOPE PLATE TEST - 5 [APT-5]?

ANOMALOSCOPE PLATE TEST - 5 [APT-5] is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K875026.

When did ANOMALOSCOPE PLATE TEST - 5 [APT-5] receive FDA 510(k) clearance?

ANOMALOSCOPE PLATE TEST - 5 [APT-5] received FDA 510(k) clearance on 1988-02-05, under 510(k) number K875026.

Who is the listed applicant for ANOMALOSCOPE PLATE TEST - 5 [APT-5]?

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 PLATE TEST - 5 [APT-5]?

The FDA product code for ANOMALOSCOPE PLATE TEST - 5 [APT-5] is HIT.

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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]K913962ANOMALOSCOPE QUADRANT TEST-6K874336PATTERN DISCRIMINATION PERIMETERK820414UNIVERSAL TESTING & ANALYSIS SYSTEMSK790109TELEMETRY, BIOMEDICALK760199ELECTRORETINOGRAPH

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Related Devices (Code: HIT)

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.

K903001SLIMCATH (TM)Gynopharma, Inc.K873908H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.Richmond Products, Inc.K873911PSEUDO ISOCHROMATIC COLOR BLINDNESS TEST BOOK - 15Richmond Products, Inc.K844694TITMUS VISION TESTER IITitmus Optical, Inc.K844365COLOR VISION TESTERSLuneau LaboratoriesK832843OSCAR COLOUR VISION TESTERKeeler Instruments, 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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