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, Selective Broth
510(k) Number K853609
Device Name APL TRYPTIC SOY BROTH
Applicant
Apl Medical Supplies
4230 S. Burnham Ave. #250
P.O. Box 14280
Las Vegas,  NV  89114
Applicant Contact JOHN WIECHEC
Correspondent
Apl Medical Supplies
4230 S. Burnham Ave. #250
P.O. Box 14280
Las Vegas,  NV  89114
Correspondent Contact JOHN WIECHEC
Regulation Number866.2360
Classification Product Code
JSD  
Date Received08/29/1985
Decision Date 09/12/1985
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
-
-