• 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 Chair, Adjustable, Mechanical
510(k) Number K874060
Device Name CONVERTA-LITTER
Applicant
Camtec
300 Muir St.
Cambridge,  MD  21613
Applicant Contact DONALD HOLDT
Correspondent
Camtec
300 Muir St.
Cambridge,  MD  21613
Correspondent Contact DONALD HOLDT
Regulation Number890.3100
Classification Product Code
INN  
Date Received10/05/1987
Decision Date 12/10/1987
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
-
-