Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Bars, Parallel, Powered
510(k) Number K932240
Device Name MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS
Applicant
Bailey Mfg. Co.
P.O. Box 130
Lodi,  OH  44254
Applicant Contact THOMAS CAMPBELL
Correspondent
Bailey Mfg. Co.
P.O. Box 130
Lodi,  OH  44254
Correspondent Contact THOMAS CAMPBELL
Regulation Number890.5380
Classification Product Code
IRR  
Date Received05/07/1993
Decision Date 04/01/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-