FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

ATLANTIS

K Number: K953936 · Decision Dec 28, 1995
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
41
Applicant Total
16
Review Days
129

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Basic Information

Device Name
ATLANTIS
K Number
K953936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1810
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trophy Radiologie
Date Received
August 21, 1995
Decision Date
December 28, 1995
Product Code
EAP
Advisory Committee
Dental
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
EAP Unit, X-Ray, Intraoral

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Other Clearances by Trophy Radiologie

K Number Device Name
K033690 TROPHYPAN AND TROPHYPAN C
K033419 STV PRO 2
K023346 TROPHYPAN
K012514 DIGIPAN / DPI
K991455 ORTHOSLICE OS1000 SERIES; PANORAMIC ORTHOSLICE OS 1000: OS1000, OS1000E PANORAMIC AND CEPHALOMETRIC ORTHOSLICE OS1000C,
K991912 MODIFICATION TO DIGIPAN
K961826 DIGIPAN
K962337 ELITYS OR ELITYS-E
K951074 STOMAVISION (STV)
K950533 TROPHY RADIOLOGIE RVG RADIOVISIOGRAPHY
Search all 16 clearances from Trophy Radiologie →