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

ORTHOPHOS AND ORTHOPHOS C

K Number: K895467 · Decision Nov 17, 1989
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
183
Applicant Total
519
Review Days
67

Basic Information

Device Name
ORTHOPHOS AND ORTHOPHOS C
K Number
K895467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Date Received
September 11, 1989
Decision Date
November 17, 1989
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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