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FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Gastroenterology and Urology
Review Panel
Cardiovascular Monitoring Devices
CFR Sub-Part
MNW
Analyzer, Body Composition
2
Product Code
K
14
0045
BODY COMPOSITION ANALYZER
2
Cleared 510(K)
K
14
1483
BIOSPACE BODY COMPOSITION ANALYZER
2
Cleared 510(K)
K
13
3872
ARIA WIFI SMART SCALE
2
Cleared 510(K)
K
14
0594
BODY FAT ANALYZER AND SCALE
2
Cleared 510(K)
K
13
0856
BIA / VITALITY ANALYZER
2
Cleared 510(K)
K
13
0777
INBODY
2
Cleared 510(K)
K
13
0952
PRECISION ONE LIFECARE; DETECTO; DETECTO
2
Cleared 510(K)
K
13
1394
TRANSTEK GLASS BODY FAT ANALYZER
2
Cleared 510(K)
K
13
0311
TRANSTEK BODY FAT ANALYZER
2
Cleared 510(K)
K
12
2388
SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514
2
Cleared 510(K)
Show All 78 Submissions
OBH
Monitor, Extracellular Fluid, Lymphedema, Extremity
2
Product Code
OMV
Ultrasonic Body Composition Analyzer
2
Product Code
PUH
Analyzer, Body Composition, Exempt
2
Product Code
QJB
Adjunct Monitor, Protein Calorie Malnutrition
2
Product Code
Diagnostic Devices
CFR Sub-Part
General Hospital and Personal Use Miscellaneous Devices
CFR Sub-Part
Miscellaneous
Miscellaneous
Monitoring Devices
CFR Sub-Part
Neurological Therapeutic Devices
CFR Sub-Part
Obstetrical and Gynecological Diagnostic Devices
CFR Sub-Part
Obstetrical and Gynecological Surgical Devices
CFR Sub-Part
Physical Medicine Therapeutic Devices
CFR Sub-Part
Prosthetic Devices
CFR Sub-Part
Surgical Devices
CFR Sub-Part
Therapeutic Devices
CFR Sub-Part
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 26 May 2023 at 11:04 pm
GU
/
cardiovascular-monitoring-devices
/
MNW
/
K122388
View Source
SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122388
510(k) Type
Traditional
Applicant
SECA GMBH & CO. KG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2013
Days to Decision
269 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
Cardiovascular Monitoring Devices
MNW
Analyzer, Body Composition
K
14
0045
BODY COMPOSITION ANALYZER
K
14
1483
BIOSPACE BODY COMPOSITION ANALYZER
K
13
3872
ARIA WIFI SMART SCALE
K
14
0594
BODY FAT ANALYZER AND SCALE
K
13
0856
BIA / VITALITY ANALYZER
K
13
0777
INBODY
K
13
0952
PRECISION ONE LIFECARE; DETECTO; DETECTO
K
13
1394
TRANSTEK GLASS BODY FAT ANALYZER
K
13
0311
TRANSTEK BODY FAT ANALYZER
K
12
2388
SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514
Show All 78 Submissions
OBH
Monitor, Extracellular Fluid, Lymphedema, Extremity
OMV
Ultrasonic Body Composition Analyzer
PUH
Analyzer, Body Composition, Exempt
QJB
Adjunct Monitor, Protein Calorie Malnutrition
Diagnostic Devices
General Hospital and Personal Use Miscellaneous Devices
Miscellaneous
Monitoring Devices
Neurological Therapeutic Devices
Obstetrical and Gynecological Diagnostic Devices
Obstetrical and Gynecological Surgical Devices
Physical Medicine Therapeutic Devices
Prosthetic Devices
Surgical Devices
Therapeutic Devices
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
GU
/
cardiovascular-monitoring-devices
/
MNW
/
K122388
View Source
SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122388
510(k) Type
Traditional
Applicant
SECA GMBH & CO. KG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2013
Days to Decision
269 days
Submission Type
Summary