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 Stand, Infusion
510(k) Number K820963
Device Name PATIENT PAL I.V. WALKER
Applicant
PRYOR PRODUCTS
420 North Cedros Avenue
Solana Beach,  CA  92075
Applicant Contact Mary Berry
Correspondent
PRYOR PRODUCTS
420 North Cedros Avenue
Solana Beach,  CA  92075
Correspondent Contact Mary Berry
Regulation Number880.6990
Classification Product Code
FOX  
Date Received04/06/1982
Decision Date 04/21/1982
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
-
-