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

IMAGERAYI

K Number: K041580 · Decision Jun 29, 2004
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
8
Review Days
15

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Basic Information

Device Name
IMAGERAYI
K Number
K041580
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Henry Schein, Inc.
Date Received
June 14, 2004
Decision Date
June 29, 2004
Product Code
MUH
Advisory Committee
Dental
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
MUH System, X-Ray, Extraoral Source, Digital

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K834056 SCHEIN COTTON ROLLS, NON-STERILE
K801079 KWIX-BITE X-RAY FILM HOLDER
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