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 Station, Pipetting And Diluting, For Clinical Use
510(k) Number K951753
Device Name MEDTEC AUTOBLOT 2000
Applicant
Medtec, Inc.
Columbia Sqare
555 Thirteenth St. NW
Washington,  DC  20004
Applicant Contact PATRICIA B SHRADER, ESQ.
Correspondent
Medtec, Inc.
Columbia Sqare
555 Thirteenth St. NW
Washington,  DC  20004
Correspondent Contact PATRICIA B SHRADER, ESQ.
Regulation Number862.2750
Classification Product Code
JQW  
Date Received04/17/1995
Decision Date 10/17/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-