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

SPECTRA FLUORESCENCE CARIES DETECTION DEVICE

K Number: K090169 · Decision Aug 18, 2009
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
18
Review Days
207

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Basic Information

Device Name
SPECTRA FLUORESCENCE CARIES DETECTION DEVICE
K Number
K090169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1745
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Air Techniques, Inc.
Date Received
January 23, 2009
Decision Date
August 18, 2009
Product Code
NBL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NBL Laser, Fluorescence Caries Detection

Similar 510(k) Clearances

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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
K052271 RINSENDO
K050693 ACCENT
K042397 SCANX 14
K042266 ACCLAIM
K031198 SCANX 10
K024285 A/T X-RAY 70
K013893 SCANX
Search all 18 clearances from Air Techniques, Inc. →