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FDA 510(k)

THE PROTECTOR

K-Number: K874412 · 1988-02-12

ApplicantTri Jon, Inc.
Decision Date1988-02-12
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Tri Jon, Inc.. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K874412. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PROTECTOR?

THE PROTECTOR is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Tri Jon, Inc.. The 510(k) number is K874412.

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

THE PROTECTOR received FDA 510(k) clearance on 1988-02-12, under 510(k) number K874412.

Who is the listed applicant for THE PROTECTOR?

The FDA 510(k) record lists Tri Jon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PROTECTOR?

The FDA product code for THE PROTECTOR is CAE.

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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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