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

ACCENT

K Number: K050693 · Decision May 26, 2005
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
18
Review Days
70

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Basic Information

Device Name
ACCENT
K Number
K050693
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Air Techniques, Inc.
Date Received
March 17, 2005
Decision Date
May 26, 2005
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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Other Clearances by Air Techniques, Inc.

K Number Device Name
K191623 ScanX Touch/ScanX Duo Touch
K190949 ScanX Barrier Envelopes
K101289 SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB
K090169 SPECTRA FLUORESCENCE CARIES DETECTION DEVICE
K052271 RINSENDO
K042397 SCANX 14
K042266 ACCLAIM
K031198 SCANX 10
K024285 A/T X-RAY 70
K013893 SCANX
Search all 18 clearances from Air Techniques, Inc. →