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

ADC DENTAL

K Number: K021542 · Decision Aug 6, 2002
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
19
Review Days
88

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Basic Information

Device Name
ADC DENTAL
K Number
K021542
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Agfa Corp.
Date Received
May 10, 2002
Decision Date
August 6, 2002
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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