Keithr Kretchmer

FDA Filings

This page includes the latest FDA filings for Keithr Kretchmer. 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
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

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