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

SOPIX 2

K Number: K092329 · Decision Jul 20, 2010
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
25
Review Days
350

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Basic Information

Device Name
SOPIX 2
K Number
K092329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sopro
Date Received
August 4, 2009
Decision Date
July 20, 2010
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 Sopro

K Number Device Name
K223470 C50
K121685 SOPROCARE
K103813 SOPRO 281
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 →