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FDA 510(k)

GENERATED RETINAL REFLEX IMAGERY SYS

K-Number: K840840 · 1984-07-12

ApplicantElectro Optical Instruments
Decision Date1984-07-12
Product CodeHKM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GENERATED RETINAL REFLEX IMAGERY SYS is the device name listed in this FDA 510(k) record. The listed applicant is Electro Optical Instruments. It received FDA 510(k) clearance on 1984-07-12 under 510(k) number K840840. The device is classified under product code HKM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERATED RETINAL REFLEX IMAGERY SYS?

GENERATED RETINAL REFLEX IMAGERY SYS is a medical device that received FDA 510(k) clearance on 1984-07-12. The listed applicant is Electro Optical Instruments. The 510(k) number is K840840.

When did GENERATED RETINAL REFLEX IMAGERY SYS receive FDA 510(k) clearance?

GENERATED RETINAL REFLEX IMAGERY SYS received FDA 510(k) clearance on 1984-07-12, under 510(k) number K840840.

Who is the listed applicant for GENERATED RETINAL REFLEX IMAGERY SYS?

The FDA 510(k) record lists Electro Optical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENERATED RETINAL REFLEX IMAGERY SYS?

The FDA product code for GENERATED RETINAL REFLEX IMAGERY SYS is HKM.

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Related Devices (Code: HKM)

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.

K964338RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOTRudolf Riester GmbH & Co. KGK950795STREAK RETINOSCOPE RX-RPNeitz Instruments Company, Ltd.K950793SPOT RETINOSCOPE RX-3SPNeitz Instruments Company, Ltd.K950791STREAK RETINOSCOPE RX-3Neitz Instruments Company, Ltd.K950792STREAK RETINOSCOPE RX-3ANeitz Instruments Company, Ltd.K950794STREAK RETINOSCOPE RX-RCNeitz Instruments Company, Ltd.

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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