KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat— 510(k) K211919

Name: FDA 510(k) clearance K211919
Creator: U.S. Food and Drug Administration
Published: 2022-03-04

Substantially Equivalent

Kinetic Innovative Seating System, LLC

FDA 510(k) clearance K211919 for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat, Substantially Equivalent on 2022-03-04. Applicant: Kinetic Innovative Seating System, LLC. Device class: 1.

Clearance details

Applicant: Kinetic Innovative Seating System, LLC
Product code: Code KNN
Device class: Class 1
Regulation: 21 CFR 890.3920
Advisory panel: Physical Medicine
Date received: 2021-06-21
Decision date: 2022-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branford, CT, US

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