VIFI: VECTOR INTERFERENTIAL ONE— 510(k) K931732

Name: FDA 510(k) clearance K931732
Creator: U.S. Food and Drug Administration
Published: 1994-03-10

Substantially Equivalent

Compliance Technology, Inc.

FDA 510(k) clearance K931732 for VIFI: VECTOR INTERFERENTIAL ONE, Substantially Equivalent on 1994-03-10. Applicant: Compliance Technology, Inc.. Device class: 2.

Clearance details

Applicant: Compliance Technology, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1993-04-07
Decision date: 1994-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murfreesboro, TN, 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

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