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FDA 510(k)

ECHO-OCULOMETER #3000

K-Number: K791766 · 1980-02-19

ApplicantJedmed Instrument Co.
Decision Date1980-02-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHO-OCULOMETER #3000 is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K791766. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO-OCULOMETER #3000?

ECHO-OCULOMETER #3000 is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K791766.

When did ECHO-OCULOMETER #3000 receive FDA 510(k) clearance?

ECHO-OCULOMETER #3000 received FDA 510(k) clearance on 1980-02-19, under 510(k) number K791766.

Who is the listed applicant for ECHO-OCULOMETER #3000?

The FDA 510(k) record lists Jedmed Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECHO-OCULOMETER #3000?

The FDA product code for ECHO-OCULOMETER #3000 is IYO.

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Other records listing Jedmed Instrument Co. 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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K953457JEDMED SPECTRUM ENT CABINETK950925JEDMED LARYNGEAL SCOPEK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

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Related Devices (Code: IYO)

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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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