FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SONOCARE

K Number: K844034 · Decision Jan 23, 1985
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
2
Applicant Total
6
Review Days
99

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Basic Information

Device Name
SONOCARE
K Number
K844034
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Echo Ultrasound
Date Received
October 16, 1984
Decision Date
January 23, 1985
Product Code
DYO
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DYO Band, Material, Orthodontic

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K872519 STERILIZED OMNI GEL
K844120 ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS