Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Innovative Seating System, LLC. It received FDA 510(k) clearance on 2022-03-04 under 510(k) 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. The listed applicant is Kinetic Innovative Seating System, LLC. The 510(k) number is K211919.

When did KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat receive FDA 510(k) clearance?

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

Who is the listed applicant for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?

The FDA 510(k) record lists Kinetic Innovative Seating System, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑