FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NHANES WHOLE BODY DXA REFERENCE DATABASE

K Number: K103265 · Decision Mar 16, 2011
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
144
Applicant Total
72
Review Days
132

Basic Information

Device Name
NHANES WHOLE BODY DXA REFERENCE DATABASE
K Number
K103265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1170
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOLOGIC, INC.
Date Received
November 4, 2010
Decision Date
March 16, 2011
Product Code
KGI
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGI Densitometer, Bone

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