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 Table, Operating-Room, Ac-Powered
510(k) Number K924700
Device Name FISK HEADREST
Applicant
Rhino Mfg.
11321 Trade Center Dr., #260
Rancho Cordova,  CA  95742
Applicant Contact SHANE FISK
Correspondent
Rhino Mfg.
11321 Trade Center Dr., #260
Rancho Cordova,  CA  95742
Correspondent Contact SHANE FISK
Regulation Number878.4960
Classification Product Code
FQO  
Date Received09/17/1992
Decision Date 01/15/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-