INTERTRON 6000/6100— 510(k) K930186

Name: FDA 510(k) clearance K930186
Creator: U.S. Food and Drug Administration
Published: 1993-07-02

Substantially Equivalent

Williams Healthcare Systems, LLC

FDA 510(k) clearance K930186 for INTERTRON 6000/6100, Substantially Equivalent on 1993-07-02. Applicant: Williams Healthcare Systems, LLC. Device class: 2.

Clearance details

Applicant: Williams Healthcare Systems, LLC
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1993-01-14
Decision date: 1993-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IMI

view all

K240788 — Ultrasound Stimulator2025-06-04
K230472 — Sonopuls 1902023-10-24
K222098 — ManaSport+2023-03-08
K210284 — ManaSport2022-04-26
K202788 — Sonomed IV, Sonomed V2021-12-23

More clearances from Williams Healthcare Systems, LLC

view all

K933443 — COMBI 2.5 INTERSEGMENTAL TRACTION TABLE1994-02-02

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