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 Labware, Assisted Reproduction
510(k) Number K991251
Device Name FALCON IVF ONE WELL DISH
Applicant
Becton Dickinson Labware
1 Becton Dr.
Franklin Lakes,  NJ  07465
Applicant Contact DAVID BALL
Correspondent
Becton Dickinson Labware
1 Becton Dr.
Franklin Lakes,  NJ  07465
Correspondent Contact DAVID BALL
Regulation Number884.6160
Classification Product Code
MQK  
Date Received04/13/1999
Decision Date 05/05/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-