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

EMPI MODEL 712, LOGIX(TM), NMS

K Number: K864010 · Decision Dec 2, 1986
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
60
Review Days
48

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EMPI MODEL 712, LOGIX(TM), NMS
K Number
K864010
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Empi
Date Received
October 15, 1986
Decision Date
December 2, 1986
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 Empi

K Number Device Name
K093324 EMPI CONTINUUM
K090922 EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATOR
K072946 HYBRESIS IONTOPHORESIS DRUG DELIVERY SYSTEM
K070427 DUPEL TRANSPORT IONTOPHORESIS SYSTEM
K061650 SELECT TENS, MODEL 4600S
K041920 INFINITY PLUS ELECTROTHERAPY SYSTEM
K042057 INFINITY ELECTROTHERAPY SYSTEM
K030395 EMPI ACTION PATCH IONTOPHORESIS SYSTEM
K021100 300 PV COMPLETE ELECTROTHERAPY SYSTEM
K991991 DUPEL IONTOPHORESIS SYSTEM
Search all 60 clearances from Empi →