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

MS-112, POWERED MUSCLE STIMULATOR

K Number: K872208 · Decision Oct 6, 1987
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
543
Applicant Total
8
Review Days
120

Basic Information

Device Name
MS-112, POWERED MUSCLE STIMULATOR
K Number
K872208
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
ELECTRO MED SUPPLY, INC.
Date Received
June 8, 1987
Decision Date
October 6, 1987
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 ELECTRO MED SUPPLY, INC.

K Number Device Name
K933368 TENS-IT
K872206 MD-104, POWERED MUSCLE STIMULATOR
K872207 MS-108, POWERED MUSCLE STIMULATOR
K862487 MS-139 ELECTRONIC MUSCLE STIMULATOR
K862486 MS-159 ELECTRONIC MUSCLE STIMULATOR
K862485 MS-179 ELECTRONIC MUSCLE STIMULATOR
K854801 MS-189 MUSCLE STIMULATOR