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FDA 510(k)

ALTON PT STEPPER

K-Number: K024183 · 2003-03-17

ApplicantAlton Design, LLC
Decision Date2003-03-17
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALTON PT STEPPER is the device name listed in this FDA 510(k) record. The listed applicant is Alton Design, LLC. It received FDA 510(k) clearance on 2003-03-17 under 510(k) number K024183. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTON PT STEPPER?

ALTON PT STEPPER is a medical device that received FDA 510(k) clearance on 2003-03-17. The listed applicant is Alton Design, LLC. The 510(k) number is K024183.

When did ALTON PT STEPPER receive FDA 510(k) clearance?

ALTON PT STEPPER received FDA 510(k) clearance on 2003-03-17, under 510(k) number K024183.

Who is the listed applicant for ALTON PT STEPPER?

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

What is the FDA product code for ALTON PT STEPPER?

The FDA product code for ALTON PT STEPPER is KXK.

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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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