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FDA 510(k)

ELECTRORETINOGRAPH

K-Number: K760199 · 1976-08-04

ApplicantLkc Technologies, Inc.
Decision Date1976-08-04
Product CodeHLZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ELECTRORETINOGRAPH 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 1976-08-04 under 510(k) number K760199. The device is classified under product code HLZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRORETINOGRAPH?

ELECTRORETINOGRAPH is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K760199.

When did ELECTRORETINOGRAPH receive FDA 510(k) clearance?

ELECTRORETINOGRAPH received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760199.

Who is the listed applicant for ELECTRORETINOGRAPH?

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 ELECTRORETINOGRAPH?

The FDA product code for ELECTRORETINOGRAPH is HLZ.

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

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Related Devices (Code: HLZ)

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.

K253586RM Electrode (RMH 25-01)Retmap, Inc.K232273RM Electrode (RMH 23-01)Retmap, Inc.K961805TOMEY DTL ELECTRODETomey Corporation USAK926540SOPHER AND BIERER OVUM FORCEPSThomasville Medical Assoc.K913239GOLDLENS(TM)Doran Instruments, Inc.K844409DTL ELECTRODESauquoit Industries, 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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