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 Full Field Digital, System, X-Ray, Mammographic
510(k) Number K220073
Device Name RMF-2000
Applicant
DRTECH Corporation
Suite # 1, 2 Floor/Suite # 2, 3 Floor, 29,
Dunchon-Daero 541beon-Gil
Jungwon-Gu, Seongnam-Si,  KR 13216
Applicant Contact Suyeon Back
Correspondent
DRTECH Corporation
Suite # 1, 2 Floor/Suite # 2, 3 Floor, 29,
Dunchon-Daero 541beon-Gil
Jungwon-Gu, Seongnam-Si,  KR 13216
Correspondent Contact Suyeon Back
Regulation Number892.1715
Classification Product Code
MUE  
Date Received01/10/2022
Decision Date 01/26/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-