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FDA 510(k)

THE EXPERIMENTAL

K-Number: K864455 · 1987-03-18

ApplicantMartin H. Kaufmann
Decision Date1987-03-18
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent for Some Indications

Device Summary

THE EXPERIMENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Martin H. Kaufmann. It received FDA 510(k) clearance on 1987-03-18 under 510(k) number K864455. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the THE EXPERIMENTAL?

THE EXPERIMENTAL is a medical device that received FDA 510(k) clearance on 1987-03-18. The listed applicant is Martin H. Kaufmann. The 510(k) number is K864455.

When did THE EXPERIMENTAL receive FDA 510(k) clearance?

THE EXPERIMENTAL received FDA 510(k) clearance on 1987-03-18, under 510(k) number K864455.

Who is the listed applicant for THE EXPERIMENTAL?

The FDA 510(k) record lists Martin H. Kaufmann as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE EXPERIMENTAL?

The FDA product code for THE EXPERIMENTAL is EFW.

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Related Devices (Code: EFW)

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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