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FDA 510(k)

EGS MODEL 300

K-Number: K790847 · 1979-05-25

ApplicantAlfred V. Greco
Decision Date1979-05-25
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EGS MODEL 300 is the device name listed in this FDA 510(k) record. The listed applicant is Alfred V. Greco. It received FDA 510(k) clearance on 1979-05-25 under 510(k) number K790847. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EGS MODEL 300?

EGS MODEL 300 is a medical device that received FDA 510(k) clearance on 1979-05-25. The listed applicant is Alfred V. Greco. The 510(k) number is K790847.

When did EGS MODEL 300 receive FDA 510(k) clearance?

EGS MODEL 300 received FDA 510(k) clearance on 1979-05-25, under 510(k) number K790847.

Who is the listed applicant for EGS MODEL 300?

The FDA 510(k) record lists Alfred V. Greco as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EGS MODEL 300?

The FDA product code for EGS MODEL 300 is IPF.

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Related Devices (Code: IPF)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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