FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MARK V HIGH VOLTAGE GALVANIC STIMULATORR

K Number: K832546 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
543
Applicant Total
11
Review Days
77

Basic Information

Device Name
MARK V HIGH VOLTAGE GALVANIC STIMULATORR
K Number
K832546
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
ORTHION CORP.
Date Received
July 29, 1983
Decision Date
October 14, 1983
Product Code
IPF
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IPF Stimulator, Muscle, Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IPF), ordered by most recent decision date.

View all

Other Clearances by ORTHION CORP.

K Number Device Name
K823149 OB TILT TABLE
K823153 BATH TUB SEAT & BATH BOARD
K823105 RESI-WALKER
K823150 SESAM TREATMENT TABLE
K823154 SHOWER STOOL W/HANDLES
K823152 OB HELP ARM
K823155 LAVATORY SEAT HEIGHTENER
K823151 OB TRIPP TRANSPORT CHAIR
K823156 COLLAPSABLE LAVATORY HEIGHTENER
K812701 ORTHO-THERM INFRARED SENSOR
Search all 11 clearances from ORTHION CORP. →