KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5— 510(k) K922695

Name: FDA 510(k) clearance K922695
Creator: U.S. Food and Drug Administration
Published: 1992-09-30

Substantially Equivalent

Kinetic Technology, Inc.

FDA 510(k) clearance K922695 for KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5, Substantially Equivalent on 1992-09-30. Applicant: Kinetic Technology, Inc.. Device class: Unclassified.

Clearance details

Applicant: Kinetic Technology, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-06-04
Decision date: 1992-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LXM

view all

K234036 — SONIK MONARK 1002024-02-15
K192629 — Spinalytics2019-12-21
K172536 — Atlas Percussion Adjusting Instrument2018-06-20
K160278 — VSTAAR AdjusteR2016-11-04
K130666 — KHAN KINETIC TREATMENT (KKT-M2)2014-01-23

More clearances from Kinetic Technology, Inc.

view all

K922692 — KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR1992-09-30
K922693 — KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-11992-09-30
K922694 — KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-41992-09-30
K870910 — PRECISION SPINAL ADJUSTER MODEL 1151988-04-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.