FDA PMA FDA Class 2 Approved 🇺🇸 United States

Bone Sonometer

PMA: P990016 · Supplement: S001 · Decision Nov 8, 2001
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Bone Sonometer
Trade Name
MC CUE PLC CUBA CLINICAL ULTRASONIC BONE SONOMETRY SYSTEM
PMA Number
P990016
Supplement Number
S001
Device Class
FDA Class 2
Product Code
MUA
Generic Name
Bone sonometer
Regulation Number
892.1180
Medical Specialty
Radiology
Advisory Committee
Radiology
Decision
Approved
Decision Code
APPR
Decision Date
November 8, 2001
Date Received
October 12, 2001
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A SOFTWARE UPDATE FROM V4.2.0 TO V4.2.1 AND A NEW PHANTOM (QA COUPLER).

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUA Bone Sonometer