FDA 510(k)

MILBURN'S BACKEASER

K-Number: K821808 · 1982-07-20

Decision Date1982-07-20

Product Code

DecisionSubstantially Equivalent

Device Summary

MILBURN'S BACKEASER is the device name listed in this FDA 510(k) record. The listed applicant is The T. Milburn Co. , Ltd.. It received FDA 510(k) clearance on 1982-07-20 under 510(k) number K821808. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILBURN'S BACKEASER?

MILBURN'S BACKEASER is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is The T. Milburn Co. , Ltd.. The 510(k) number is K821808.

When did MILBURN'S BACKEASER receive FDA 510(k) clearance?

MILBURN'S BACKEASER received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821808.

Who is the listed applicant for MILBURN'S BACKEASER?

The FDA 510(k) record lists The T. Milburn Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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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.