INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2— 510(k) K921612

Name: FDA 510(k) clearance K921612
Creator: U.S. Food and Drug Administration
Published: 1992-08-18

Substantially Equivalent

Medstar, Inc.

FDA 510(k) clearance K921612 for INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2, Substantially Equivalent on 1992-08-18. Applicant: Medstar, Inc.. Device class: 2.

Clearance details

Applicant: Medstar, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1992-04-03
Decision date: 1992-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Olathe, KS, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIH

view all

K231575 — Vecttor VT-3002024-02-08
K202725 — ETD40002021-03-26
K183692 — Avid IF22019-06-12
K122944 — GEMORE TRUE SINE INTERFERENTIAL STIMULATOR2012-12-21
K121662 — VECTTOR VT-2002012-11-21

More clearances from Medstar, Inc.

view all

K880548 — SAFE-STRIPS1988-09-29

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