FDA 510(k)

HEMAWAY SEAT

K-Number: K072690 · 2007-12-07

Decision Date2007-12-07

Product CodeLRL

DecisionSubstantially Equivalent

Device Summary

HEMAWAY SEAT is the device name listed in this FDA 510(k) record. The listed applicant is Hemaway, LLC. It received FDA 510(k) clearance on 2007-12-07 under 510(k) number K072690. The device is classified under product code LRL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMAWAY SEAT?

HEMAWAY SEAT is a medical device that received FDA 510(k) clearance on 2007-12-07. The listed applicant is Hemaway, LLC. The 510(k) number is K072690.

When did HEMAWAY SEAT receive FDA 510(k) clearance?

HEMAWAY SEAT received FDA 510(k) clearance on 2007-12-07, under 510(k) number K072690.

Who is the listed applicant for HEMAWAY SEAT?

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

What is the FDA product code for HEMAWAY SEAT?

The FDA product code for HEMAWAY SEAT is LRL.

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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.