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

CS 7600

K Number: K111649 · Decision Sep 23, 2011
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
48
Review Days
102

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Basic Information

Device Name
CS 7600
K Number
K111649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carestream Health, Inc.
Date Received
June 13, 2011
Decision Date
September 23, 2011
Product Code
MUH
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
MUH System, X-Ray, Extraoral Source, Digital

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K202441 Eclipse II with Smart Noise Cancellation
K201373 DRX-Compass
K192894 Vita Flex CR System with LLI
K193574 Q-Rad System
K191879 DRX-Evolution with Carestream Digital Tomosynthesis
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