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GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072439
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2007
Days to Decision
15 days
Submission Type
Summary

GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072439
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2007
Days to Decision
15 days
Submission Type
Summary