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

SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE

K Number: K131906 · Decision Apr 11, 2014
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
11
Review Days
289

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Basic Information

Device Name
SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE
K Number
K131906
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Satelec - Acteon Group
Date Received
June 26, 2013
Decision Date
April 11, 2014
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

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Other Clearances by Satelec - Acteon Group

K Number Device Name
K233922 SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG
K172137 PIEZOTOME CUBE
K132322 NEWTRON P5 XS B.LED
K132267 NEWTRON P5, NEWTRON P5 B.LED
K131151 ENDOCENTER
K131997 NEWTRON BOOSTER
K113430 PROULTRA PIEZO ULTRASONIC
K111623 I-ENDO DUAL
K072030 IMPLANT CENTER
K071424 PMAX NEWTRON XS
Search all 11 clearances from Satelec - Acteon Group →