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 Diluent, Blood Cell
510(k) Number K851280
Device Name DASS PACK
Applicant
Dass, Inc.
Diag. Assoc. Services & Sales
155a New Boston St.
Woburn,  MA  01801
Applicant Contact FRANK F CALO
Correspondent
Dass, Inc.
Diag. Assoc. Services & Sales
155a New Boston St.
Woburn,  MA  01801
Correspondent Contact FRANK F CALO
Regulation Number864.8200
Classification Product Code
GIF  
Date Received04/01/1985
Decision Date 07/05/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-