FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FLEXISCOPE OPTOMODUL

K Number: K984641 · Decision Mar 29, 1999
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
12
Review Days
88

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Basic Information

Device Name
FLEXISCOPE OPTOMODUL
K Number
K984641
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Schoelly Fiberoptic GmbH
Date Received
December 31, 1998
Decision Date
March 29, 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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K143673 CMOS Video Nasopharyngoscope System
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K132009 CMOS VIDEO NASOPHARYNGOSCOPE SYSTEM
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