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

EV APAN DIGITAL, MODEL K1VSM2000

K Number: K041120 · Decision Aug 30, 2004
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
13
Review Days
123

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Basic Information

Device Name
EV APAN DIGITAL, MODEL K1VSM2000
K Number
K041120
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Afp Imaging Corp.
Date Received
April 29, 2004
Decision Date
August 30, 2004
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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K013176 MODIFICATION TO: SENS-A-RAY SYSTEM WITH PROIMAGE SOFTWARE
K974619 SCANARAY/CD-DENT ADVANCED COMPUTERIZED X-RAY SYSTEM
K950288 AUTOLASER MULTI FORMAT CAMERA
K925885 AFP 17 X 4 AUTOMATIC FILM PROCESSOR
K930761 IMAGE-X 70 INTRAORAL X-RAY SYSTEM
K925684 OLYMP-X,X-RAY GENERATOR
Search all 13 clearances from Afp Imaging Corp. →