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FDA 510(k)

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat

K-Number: K211919 · 2022-03-04

ApplicantKinetic Innovative Seating System, LLC
Decision Date2022-03-04
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is a medical device manufactured by Kinetic Innovative Seating System, LLC. It received FDA 510(k) clearance on 2022-03-04 under approval number K211919. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is a medical device that received FDA 510(k) clearance on 2022-03-04. It is manufactured by Kinetic Innovative Seating System, LLC. The 510(k) number is K211919.

When was KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat approved by the FDA?

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat received FDA 510(k) clearance on 2022-03-04, under approval number K211919.

What company makes KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is manufactured by Kinetic Innovative Seating System, LLC.

What is the FDA product code for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?

The FDA product code for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is KNN.

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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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