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FDA 510(k)

POST-AID

K-Number: K840907 · 1984-08-02

ApplicantE.W. Link, Inc.
Decision Date1984-08-02
Product CodeKCM
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

POST-AID is the device name listed in this FDA 510(k) record. The listed applicant is E.W. Link, Inc.. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K840907. The device is classified under product code KCM. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST-AID?

POST-AID is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is E.W. Link, Inc.. The 510(k) number is K840907.

When did POST-AID receive FDA 510(k) clearance?

POST-AID received FDA 510(k) clearance on 1984-08-02, under 510(k) number K840907.

Who is the listed applicant for POST-AID?

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

What is the FDA product code for POST-AID?

The FDA product code for POST-AID is KCM.

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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