• 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 micromanipulators and microinjectors, assisted reproduction
510(k) Number K010298
Device Name MN-4 COARSE MANIPULATOR
Applicant
NARISHIGE CO., LTD.
27-9 MINAMIKARASUYAMA 4-CHOME
SETAGAYA-KU, TOKYO,  JP 157-0062
Applicant Contact MITSUKO YONEYAMA
Correspondent
NARISHIGE CO., LTD.
27-9 MINAMIKARASUYAMA 4-CHOME
SETAGAYA-KU, TOKYO,  JP 157-0062
Correspondent Contact MITSUKO YONEYAMA
Regulation Number884.6150
Classification Product Code
MQJ  
Date Received01/31/2001
Decision Date 03/16/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-