• 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 Kit, Identification, Glucose Nonfermenter
510(k) Number K900517
Device Name RAPID NF SYSTEM
Applicant
Innovative Diagnostic Systems, Inc.
3404 Oakcliff Rd. #C-1
Atlanta,  GA  30340
Applicant Contact LOUIS A ERIQUEZ,PHD
Correspondent
Innovative Diagnostic Systems, Inc.
3404 Oakcliff Rd. #C-1
Atlanta,  GA  30340
Correspondent Contact LOUIS A ERIQUEZ,PHD
Regulation Number866.2660
Classification Product Code
JSW  
Date Received02/02/1990
Decision Date 03/13/1990
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
-
-