ELECTRO-NERVE STIMULATOR TENS MODEL,INF 4150/A— 510(k) K905571

Name: FDA 510(k) clearance K905571
Creator: U.S. Food and Drug Administration
Published: 1991-05-08

Substantially Equivalent

Biomedical Life Systems, Inc.

FDA 510(k) clearance K905571 for ELECTRO-NERVE STIMULATOR TENS MODEL,INF 4150/A, Substantially Equivalent on 1991-05-08. Applicant: Biomedical Life Systems, Inc.. Device class: 2.

Clearance details

Applicant: Biomedical Life Systems, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1990-12-12
Decision date: 1991-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Marcos, CA, 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 Biomedical Life Systems, Inc.

view all

K172971 — BMLS16-12018-07-08
K102051 — PAIN BUDDY2011-07-29
K061476 — ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-12006-07-26
K042711 — MODEL BMLS03-72005-03-14
K041388 — COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-12004-11-23

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