FDA 510(k)

EF2000

K-Number: K820953 · 1982-07-22

Decision Date1982-07-22

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

EF2000 is the device name listed in this FDA 510(k) record. The listed applicant is Squire, Sanders & Dempsey. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K820953. 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 EF2000?

EF2000 is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Squire, Sanders & Dempsey. The 510(k) number is K820953.

When did EF2000 receive FDA 510(k) clearance?

EF2000 received FDA 510(k) clearance on 1982-07-22, under 510(k) number K820953.

Who is the listed applicant for EF2000?

The FDA 510(k) record lists Squire, Sanders & Dempsey as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EF2000?

The FDA product code for EF2000 is IPF.

Other records listing Squire, Sanders & Dempsey 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.

K821449P6S ATHLETIC

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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.