• 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 Bed, Flotation Therapy, Powered
510(k) Number K910851
Device Name TASSI MK3 (TURNAIR)
Applicant
Therapy Air Support Systems, Inc.
13912 Ponderosa, Unit-H
Santa Ana,  CA  92705
Applicant Contact BILL ROSS
Correspondent
Therapy Air Support Systems, Inc.
13912 Ponderosa, Unit-H
Santa Ana,  CA  92705
Correspondent Contact BILL ROSS
Regulation Number890.5170
Classification Product Code
IOQ  
Date Received02/28/1991
Decision Date 05/15/1991
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
-
-