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 Syringe, Piston
510(k) Number K893233
Device Name DISPOSABLE NEEDLE, ASPIRATION AND INJECTION
Applicant
Pioneer Intl. Co.
5550 Penland Rd.,
Hidden Hills,  CA  91302
Applicant Contact DAVID HSIUNG
Correspondent
Pioneer Intl. Co.
5550 Penland Rd.,
Hidden Hills,  CA  91302
Correspondent Contact DAVID HSIUNG
Regulation Number880.5860
Classification Product Code
FMF  
Date Received04/28/1989
Decision Date 01/04/1990
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
-
-