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 Stretcher, Wheeled
510(k) Number K933060
Device Name S-610 & 2-628 WHEELED SHOWER STRETCHERS
Applicant
The Anthros Medical Group
807 E. Spring
Highland,  KS  66035
Applicant Contact NANCY BABCOCK
Correspondent
The Anthros Medical Group
807 E. Spring
Highland,  KS  66035
Correspondent Contact NANCY BABCOCK
Regulation Number880.6910
Classification Product Code
FPO  
Date Received06/22/1993
Decision Date 02/04/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-