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FDA 510(k)

EPIC D215

K-Number: K790574 · 1979-04-30

ApplicantNational Patent Development Corp.
Decision Date1979-04-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EPIC D215 is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1979-04-30 under 510(k) number K790574. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPIC D215?

EPIC D215 is a medical device that received FDA 510(k) clearance on 1979-04-30. The listed applicant is National Patent Development Corp.. The 510(k) number is K790574.

When did EPIC D215 receive FDA 510(k) clearance?

EPIC D215 received FDA 510(k) clearance on 1979-04-30, under 510(k) number K790574.

Who is the listed applicant for EPIC D215?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPIC D215?

The FDA product code for EPIC D215 is FPA.

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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.

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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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