FDA.reportPublic FDA data

510(k) K932240

Device
MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS
Applicant
BAILEY MFG. CO.
510(k) number
K932240
Product code
IRR  
Decision
Substantially Equivalent (SESE)
Decision date
1994-04-01
Date received
1993-05-07
Regulation
890.5380
Classification name
Bars, Parallel, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
THOMAS CAMPBELL
Address
P.O. Box 130 Lodi OH US 44254 44254

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases