Mikasa X Ray Co L T D

FDA Filings

This page includes the latest FDA filings for Mikasa X Ray Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number9610982
FEI Number3002807605
NameKEITHR.KRETCHMER
Owner & OperatorMIKASA X-RAY CO., LTD.
Contact Address5-10-5, KOISHIKAWA, BUNKYO-KU --
TOKYO JP-13 Tokyo 112-0002 JP
Official Correspondent
  • SHUJI - SHINAGAWA
  • 81-3-38116958-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3611 COMMERCIAL AVE.
NORTHBROOK, IL 60062 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
TR90BH portable battery operated medical x-ray unit2019-01-04
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
HF1202H PowerPlus2016-08-19
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray HFP402007-11-12
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray HFP242007-11-12
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray P200D Mark III2007-11-01
MIKASA X-RAY CO., LTD.
MINXRAY, MODELS HFP24 AND HFP402006-04-05
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray HF70DUL Type A2001-10-22
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray HF100H+1979-04-26
KEITHR.KRETCHMER [MIKASA X-RAY CO., LTD.]
MinXray HF120/60HPPWV1979-04-26

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.