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 Susceptibility Test Discs, Antimicrobial
510(k) Number K810427
Device Name CEFOTAXIME 30MCG ANTIMICROBIAL SUSCEP.
Applicant
Pfizer Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Pfizer Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.1620
Classification Product Code
JTN  
Date Received02/18/1981
Decision Date 03/31/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-