FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE

K Number: K901035 · Decision Apr 23, 1990
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
44
Applicant Total
17
Review Days
48

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Basic Information

Device Name
FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE
K Number
K901035
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cuda Products Co.
Date Received
March 6, 1990
Decision Date
April 23, 1990
Product Code
FST
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FST Light, Surgical, Fiberoptic

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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
K943731 VIDEO OTOSCOPE
K935818 ENDOSCOPE
K933369 CUDA PRODUCTS CORP. LIGHTSOURCES
Search all 17 clearances from Cuda Products Co. →