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

INTRAORAL VIDEO SCOPE AND WINDOW TUBE

K Number: K951019 · Decision May 10, 1995
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
17
Review Days
64

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Basic Information

Device Name
INTRAORAL VIDEO SCOPE AND WINDOW TUBE
K Number
K951019
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cuda Products Co.
Date Received
March 7, 1995
Decision Date
May 10, 1995
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 Cuda Products Co.

K Number Device Name
K983277 LIGHTSOURCE OR ILLUMINATOR MODEL I-100
K981962 CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE
K981469 CERMAX300 LIGHTSOURCE
K980350 VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150
K980166 LIGHTSOURCE OR ILLUMINATOR
K961074 LIGHTSOURCE OR ILLUMINATOR
K943731 VIDEO OTOSCOPE
K935818 ENDOSCOPE
K933369 CUDA PRODUCTS CORP. LIGHTSOURCES
K934337 CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE
Search all 17 clearances from Cuda Products Co. →