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PCS
Liver Iron Concentration Imaging Companion Diagnostic For Deferasirox
2
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PDK
Cream For X-Ray Attenuation
2
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QBS
Radiological Computer Assisted Detection/Diagnosis Software For Fracture
2
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K
24
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Show All 23 Submissions
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Generator, Measurement, And/Or Delivery System For Hyperpolarized Mr Imaging Agents And Accessories, Cder Or Cber-Led
N
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2
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Radiology Software For Opportunistic Evaluation Of Low Bone Mineral Density
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Last synced on 20 December 2024 at 11:05 pm
RA
/
RA-misc
/
QDQ
/
K212783
View Source
ProstatID
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212783
510(k) Type
Traditional
Applicant
ScanMed, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2022
Days to Decision
310 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
Miscellaneous
PCS
Liver Iron Concentration Imaging Companion Diagnostic For Deferasirox
PDK
Cream For X-Ray Attenuation
QBS
Radiological Computer Assisted Detection/Diagnosis Software For Fracture
QDQ
Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer
K
24
1747
Saige-Dx
K
24
0417
ProFound Detection (V4.0)
K
24
2652
Lunit INSIGHT DBT v1.1
K
24
0697
See-Mode Augmented Reporting Tool, Thyroid (SMART-T)
K
24
0301
MammoScreen® (3)
K
23
1470
Lunit INSIGHT DBT
K
23
0096
Genius AI Detection 2.0 with CC-MLO Correlation
K
22
1449
Genius AI Detection 2.0
K
22
1347
Transpara 1.7.2
K
21
2783
ProstatID
Show All 23 Submissions
QJU
Image Acquisition And/Or Optimization Guided By Artificial Intelligence
QRN
Radiation Therapy Marking Device
KTA
Medium, Contrast, Radiologic
LMZ
Applicator, Hyperthermia, Interstitial
LNB
Applicator, Hyperthermia, Deep Heating, Ultrasound
LNC
Applicator, Hyperthermia, Superficial, Rf/Microwave
LOC
System, Rf/Microwave Hyperthermia, Cancer Treatment
LSY
Ultrasound, Hyperthermia, Cancer Treatment
MJS
Contrast Media, Ultrasound
MOT
Irradiator, Blood To Prevent Graft Versus Host Disease
NAN
Tester, Acoustic, Bone Quality
NAW
Microspheres Radionuclide
NCL
Imager, Breast, Electrical Impedance
OLQ
Cross-Sectional Mammographic Xray System
OTE
Digital Breast Tomosynthesis
PAA
Automated Breast Ultrasound
QNK
Optoacoustic Imaging System
QUV
Phase-Changing Fiducial Marker For Radiation Therapy
QVA
Fludeoxyglucose F18-Guided Radiation Therapy System
QVD
Radiological Machine Learning Based Quantitative Imaging Software With Change Control Plan
QXR
Vaginal Hydrogel Packing System
QVW
Generator, Measurement, And/Or Delivery System For Hyperpolarized Mr Imaging Agents And Accessories, Cder Or Cber-Led
QZL
Post-Ablation Tissue Response Prediction Software
QWO
Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.
SAO
Radiology Software For Opportunistic Evaluation Of Low Bone Mineral Density
Submissions with No Product Code
Subpart B—Diagnostic Devices
Subpart C—Obstetrical and Gynecological Monitoring Devices
Subpart F—Therapeutic Devices
Subpart G—Miscellaneous Devices
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
RA
/
RA-misc
/
QDQ
/
K212783
View Source
ProstatID
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212783
510(k) Type
Traditional
Applicant
ScanMed, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2022
Days to Decision
310 days
Submission Type
Summary