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

LIGHTSOURCE OR ILLUMINATOR

K Number: K980166 · Decision Apr 1, 1998
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
17
Review Days
75

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Basic Information

Device Name
LIGHTSOURCE OR ILLUMINATOR
K Number
K980166
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cuda Products Co.
Date Received
January 16, 1998
Decision Date
April 1, 1998
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HET), 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
K961074 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. →