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 Chair, With Casters
510(k) Number K941738
Device Name STRYKER 5050 STRECHAIR
Applicant
Stryker Medical
6300 S. Sprinkle Rd.
Kalamazoo,  MI  49001
Applicant Contact CHAD COBERLY
Correspondent
Stryker Medical
6300 S. Sprinkle Rd.
Kalamazoo,  MI  49001
Correspondent Contact CHAD COBERLY
Regulation Number890.3100
Classification Product Code
INM  
Date Received04/07/1994
Decision Date 05/06/1994
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
-
-