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 Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
510(k) Number K130056
Device Name PATIENT MONITOR
Applicant
LD TECHNOLOGY LLC
100 N. BISCAYNE BLVD, STE 502
MIAMI,  FL  33132
Applicant Contact ALBERT MAAREK
Correspondent
LD TECHNOLOGY LLC
100 N. BISCAYNE BLVD, STE 502
MIAMI,  FL  33132
Correspondent Contact ALBERT MAAREK
Regulation Number870.2300
Classification Product Code
MWI  
Date Received01/09/2013
Decision Date 04/11/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-