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FDA 510(k)

ELECTROTHERAPY APPARATUS E.T. 720

K-Number: K770276 · 1977-03-09

ApplicantFort & Assoc.
Decision Date1977-03-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTROTHERAPY APPARATUS E.T. 720 is the device name listed in this FDA 510(k) record. The listed applicant is Fort & Assoc.. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770276. 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 ELECTROTHERAPY APPARATUS E.T. 720?

ELECTROTHERAPY APPARATUS E.T. 720 is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Fort & Assoc.. The 510(k) number is K770276.

When did ELECTROTHERAPY APPARATUS E.T. 720 receive FDA 510(k) clearance?

ELECTROTHERAPY APPARATUS E.T. 720 received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770276.

Who is the listed applicant for ELECTROTHERAPY APPARATUS E.T. 720?

The FDA 510(k) record lists Fort & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROTHERAPY APPARATUS E.T. 720?

The FDA product code for ELECTROTHERAPY APPARATUS E.T. 720 is IPF.

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Related Devices (Code: IPF)

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

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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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