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

VIDEO OTOSCOPE

K Number: K943731 · Decision Oct 11, 1994
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
55
Applicant Total
17
Review Days
70

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Basic Information

Device Name
VIDEO OTOSCOPE
K Number
K943731
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4770
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cuda Products Co.
Date Received
August 2, 1994
Decision Date
October 11, 1994
Product Code
ERA
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ERA Otoscope

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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
K951019 INTRAORAL VIDEO SCOPE AND WINDOW TUBE
K935818 ENDOSCOPE
K933369 CUDA PRODUCTS CORP. LIGHTSOURCES
K934337 CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE
Search all 17 clearances from Cuda Products Co. →