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 Set, Administration, Intravascular
510(k) Number K894787
Device Name MEL-PAK GENERAL DRUG DELIVERY SYSTEM KIT
Applicant
New York Blood Center, Inc.
Box 5119
155 Duryea Rd.
Melville,  NY  11747
Applicant Contact MARTIN H STRYKER
Correspondent
New York Blood Center, Inc.
Box 5119
155 Duryea Rd.
Melville,  NY  11747
Correspondent Contact MARTIN H STRYKER
Regulation Number880.5440
Classification Product Code
FPA  
Date Received07/31/1989
Decision Date 09/13/1989
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
-
-