• 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 Set, Administration, Intravascular
510(k) Number K861519
Device Name UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)
Applicant
JUFREY MULTIMED CORP.
ATTN: IRA FISHMAN
2550 M STREET, N.W.
WASHINGTON,  DC  20037
Applicant Contact & BLOW
Correspondent
JUFREY MULTIMED CORP.
ATTN: IRA FISHMAN
2550 M STREET, N.W.
WASHINGTON,  DC  20037
Correspondent Contact & BLOW
Regulation Number880.5440
Classification Product Code
FPA  
Date Received04/23/1986
Decision Date 05/27/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-