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 Culture Media, Antimicrobial Susceptibility Test
510(k) Number K872686
Device Name IAFP MUELLER HINTON AGAR
Applicant
I.A.F. Production, Inc.
527, Boul. Des Prairies
Laval, Que. H7n-423,  CA
Applicant Contact FRANCOIS MORIN
Correspondent
I.A.F. Production, Inc.
527, Boul. Des Prairies
Laval, Que. H7n-423,  CA
Correspondent Contact FRANCOIS MORIN
Regulation Number866.1700
Classification Product Code
LKA  
Date Received07/07/1987
Decision Date 08/11/1987
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
-
-