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FDA 510(k)

STEPMILL EXERCISE SYSTEM

K-Number: K926170 · 1993-03-31

ApplicantStairmaster Sports/Medical Products, Inc.
Decision Date1993-03-31
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STEPMILL EXERCISE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stairmaster Sports/Medical Products, Inc.. It received FDA 510(k) clearance on 1993-03-31 under 510(k) number K926170. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEPMILL EXERCISE SYSTEM?

STEPMILL EXERCISE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Stairmaster Sports/Medical Products, Inc.. The 510(k) number is K926170.

When did STEPMILL EXERCISE SYSTEM receive FDA 510(k) clearance?

STEPMILL EXERCISE SYSTEM received FDA 510(k) clearance on 1993-03-31, under 510(k) number K926170.

Who is the listed applicant for STEPMILL EXERCISE SYSTEM?

The FDA 510(k) record lists Stairmaster Sports/Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEPMILL EXERCISE SYSTEM?

The FDA product code for STEPMILL EXERCISE SYSTEM is ISD.

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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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