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 Elevator, Wheelchair, Portable
510(k) Number K920105
Device Name SCALAMOBIL
Applicant
Alber Technologies, Inc.
C/O Arent/Fox/Kinter/Plot/Kahn
1050 Connecticut Ave., NW
Washington,  DC  20036
Applicant Contact MINDY L KLASKY
Correspondent
Alber Technologies, Inc.
C/O Arent/Fox/Kinter/Plot/Kahn
1050 Connecticut Ave., NW
Washington,  DC  20036
Correspondent Contact MINDY L KLASKY
Regulation Number890.3930
Classification Product Code
ING  
Date Received01/09/1992
Decision Date 08/06/1992
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
-
-