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 System, Telethermographic (Adjunctive Use)
510(k) Number K181716
Device Name InTouch Thermal Camera
Applicant
Intouch Technologies, Inc., D.B.A. Intouch Health
7402 Hollister Ave.
Goleta,  CA  93117
Applicant Contact Karen Mullin
Correspondent
Intouch Technologies, Inc., D.B.A. Intouch Health
7402 Hollister Ave.
Goleta,  CA  93117
Correspondent Contact Karen Mullin
Regulation Number884.2980
Classification Product Code
LHQ  
Date Received06/28/2018
Decision Date 03/25/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-