FDA 510(k), K952683, APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE

510(K) Number: K952683
Device Name: APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE
Manufacturer: SUSAN D GOLDSTEIN-FALK
Device Classification Name: Interferential Current Therapy
Regulation Number: LIH
Classification Product Code: KXA
Date Received: 06/12/1995
Decision Date: 04/01/1997
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology

110 pages (77 of 187 original pages are fully redacted)