Anesthesiology
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart C—Obstetrical and Gynecological Monitoring DevicesCFR Sub-Part
- IYMSystem, Telethermographic, Infrared3Product Code
- KXZSystem, Thermographic, Liquid Crystal, Powered (Adjunctive Use)3Product Code
- KYASystem, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use)1Product Code
- LHMSystem, Thermographic, Liquid Crystal1Product Code
- LHPSystem, Telethermographic (Sole Diagnostic Screen)3Product Code
- LHQSystem, Telethermographic (Adjunctive Use)1Product Code
- K232462ThermPix Thermovisual Camera1Cleared 510(K)
- K213650ThermPix Thermovisual Camera1Cleared 510(K)
- K212965Smile-100 System1Cleared 510(K)
- K212412IRIS-XP1Cleared 510(K)
- K200999Thermidas IR System (ThIR-A615)1Cleared 510(K)
- K181716InTouch Thermal Camera1Cleared 510(K)
- K171928Med-Hot Thermal Imaging Systems1Cleared 510(K)
- K162767Sentinel BreastScan II System1Cleared 510(K)
- K160573FirstSense Breast Exam1Cleared 510(K)
- K150457AlfaSight 9000 Thermographic System1Cleared 510(K)
Show All 40 Submissions
- LHRSystem, Thermographic, Liquid Crystal (Sole Diagnostic Screen)3Product Code
- LXEDoppler, Fetal, Ultrasound2Product Code
- MAAMonitor, Fetal Doppler Ultrasound2Product Code
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
InTouch Thermal Camera
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- Analyzed PDF
- 510(k) Number
- K181716
- 510(k) Type
- Traditional
- Applicant
- Intouch Technologies, Inc., D.B.A. Intouch Health
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 3/25/2019
- Days to Decision
- 270 days
- Submission Type
- Summary