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

LIGHTSOURCE OR ILLUMINATOR

K Number: K961074 · Decision Apr 30, 1996
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
19
Applicant Total
17
Review Days
43

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Basic Information

Device Name
LIGHTSOURCE OR ILLUMINATOR
K Number
K961074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cuda Products Co.
Date Received
March 18, 1996
Decision Date
April 30, 1996
Product Code
FSS
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
FSS Light, Surgical, Floor Standing

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FSS), ordered by most recent decision date.

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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
K951019 INTRAORAL VIDEO SCOPE AND WINDOW TUBE
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. →