FDA 510(k) FDA class 1 Substantially Equivalent 🇫🇷 France

S555 INTRAORAL DENTAL CAMERA

K Number: K983625 · Decision Jan 11, 1999
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
25
Review Days
88

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Basic Information

Device Name
S555 INTRAORAL DENTAL CAMERA
K Number
K983625
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sopro
Date Received
October 15, 1998
Decision Date
January 11, 1999
Product Code
EIA
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
EIA Unit, Operative Dental

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Other Clearances by Sopro

K Number Device Name
K223470 C50
K121685 SOPROCARE
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
Search all 25 clearances from Sopro →