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, Breathing Frequency
510(k) Number K243183
Device Name RTMsense Respiratory Monitoring System
Applicant
Rtm Vital Signs, LLC
8 Richards Way
Ambler,  PA  19002 -2532
Applicant Contact Dicciani Nance
Correspondent
Mededge Consulting
7005 Evergreen Place
Roswell,  GA  30076
Correspondent Contact Billi-Jo Pfalzgraf
Regulation Number868.2375
Classification Product Code
BZQ  
Date Received09/30/2024
Decision Date 06/27/2025
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-