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

SOPROCARE

K Number: K121685 · Decision Mar 12, 2013
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
25
Review Days
278

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Basic Information

Device Name
SOPROCARE
K Number
K121685
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1745
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sopro
Date Received
June 7, 2012
Decision Date
March 12, 2013
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

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Other Clearances by Sopro

K Number Device Name
K223470 C50
K103813 SOPRO 281
K092329 SOPIX 2
K092583 SOPROLIFE
K082796 SOPRO 184 CAMERA
K080122 SOPRO 670 ARTHROSCOPIC PUMP
K070783 SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR
K072912 SOPRO 225 DUAL HALOGEN LIGHT SOURCE
K070102 SOPRO 162 CAMERA
K031593 SOPRO 61D
Search all 25 clearances from Sopro →