• 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 Tubes, Vials, Systems, Serum Separators, Blood Collection
510(k) Number K893613
Device Name STATSPIN MINI-PLASMA
Applicant
Statspin Technologies
85 Morse St.
Norwood,  MA  02062
Applicant Contact THOMAS KELLEY
Correspondent
Statspin Technologies
85 Morse St.
Norwood,  MA  02062
Correspondent Contact THOMAS KELLEY
Regulation Number862.1675
Classification Product Code
JKA  
Date Received05/10/1989
Decision Date 08/28/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-