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510(k) K040824

INTERFERENTIAL STIMULATOR, MODEL BMLS03-6 by Biomedical Life Systems, Inc. — Product Code LIH

K040824 is an FDA 510(k) premarket notification submitted by Biomedical Life Systems, Inc. for the device "INTERFERENTIAL STIMULATOR, MODEL BMLS03-6". The FDA issued a decision of Substantially Equivalent on April 29, 2004. The device falls under product code LIH (Interferential Current Therapy), a Class II device regulated under 21 CFR 882.5890. Biomedical Life Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 2004
Date Received
March 30, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Interferential Current Therapy
Device Class
Class II
Regulation Number
882.5890
Review Panel
NE
Submission Type

Other clearances by Biomedical Life Systems, Inc.

  • K172971 — BMLS16-1 (July 8, 2018)
  • K102051 — PAIN BUDDY (July 29, 2011)
  • K061476 — ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1 (July 26, 2006)
  • K042711 — MODEL BMLS03-7 (March 14, 2005)
  • K041388 — COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, (November 23, 2004)
  • K040007 — INTERFERENTIAL STIMULATOR, MODEL BMLS02-6 (July 7, 2004)
  • K033174 — BMLS03-3 (June 30, 2004)
  • K040306 — HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 (March 23, 2004)
  • K033455 — ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 (January 15, 2004)
  • K031427 — ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1 (August 19, 2003)

Other clearances for product code LIH

  • K231575 — Vecttor VT-300 (February 8, 2024)
  • K202725 — ETD4000 (March 26, 2021)
  • K183692 — Avid IF2 (June 12, 2019)
  • K122944 — GEMORE TRUE SINE INTERFERENTIAL STIMULATOR (December 21, 2012)
  • K121662 — VECTTOR VT-200 (November 21, 2012)
  • K110509 — EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 (June 20, 2011)
  • K100246 — MAX-IF1000 (November 24, 2010)
  • K092780 — INF 4160 PLUS, MODEL D-FJ31F (January 7, 2010)
  • K092763 — IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D (October 8, 2009)
  • K090023 — IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E (January 30, 2009)

FDA data resources