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

SIEMENS ORTHOPHOS DS/DS CEPH

K Number: K972312 · Decision Sep 15, 1997
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
15
Review Days
87

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Basic Information

Device Name
SIEMENS ORTHOPHOS DS/DS CEPH
K Number
K972312
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Siemens AG
Date Received
June 20, 1997
Decision Date
September 15, 1997
Product Code
EHD
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
EHD Unit, X-Ray, Extraoral With Timer

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