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FDA 510(k)

STEPPING KINEMATIC IMAGING PLATFORM (SKIP)

K-Number: K992892 · 1999-09-16

ApplicantMagnetic Moments, LLC
Decision Date1999-09-16
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STEPPING KINEMATIC IMAGING PLATFORM (SKIP) is the device name listed in this FDA 510(k) record. The listed applicant is Magnetic Moments, LLC. It received FDA 510(k) clearance on 1999-09-16 under 510(k) number K992892. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEPPING KINEMATIC IMAGING PLATFORM (SKIP)?

STEPPING KINEMATIC IMAGING PLATFORM (SKIP) is a medical device that received FDA 510(k) clearance on 1999-09-16. The listed applicant is Magnetic Moments, LLC. The 510(k) number is K992892.

When did STEPPING KINEMATIC IMAGING PLATFORM (SKIP) receive FDA 510(k) clearance?

STEPPING KINEMATIC IMAGING PLATFORM (SKIP) received FDA 510(k) clearance on 1999-09-16, under 510(k) number K992892.

Who is the listed applicant for STEPPING KINEMATIC IMAGING PLATFORM (SKIP)?

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

What is the FDA product code for STEPPING KINEMATIC IMAGING PLATFORM (SKIP)?

The FDA product code for STEPPING KINEMATIC IMAGING PLATFORM (SKIP) is LNH.

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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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