Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
- HematologyReview Panel
- ImmunologyReview Panel
- MicrobiologyReview Panel
- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- 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
- 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
ELC-THERMO-SYSTEM
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- Analyzed PDF
- 510(k) Number
- K770678
- 510(k) Type
- Traditional
- Applicant
- CUTTER LABORATORIES, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 5/25/1977
- Days to Decision
- 44 days