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

HAWK INTRAORAL CAMERA AND ACCESSORIES

K Number: K040116 · Decision Apr 20, 2004
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
6
Review Days
91

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Basic Information

Device Name
HAWK INTRAORAL CAMERA AND ACCESSORIES
K Number
K040116
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dxm Co., Ltd.
Date Received
January 20, 2004
Decision Date
April 20, 2004
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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