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

CYSTOTOME, 140-S

K Number: K840475 · Decision Apr 5, 1984
Classifications
1
FEI Numbers
80
Registration Numbers
81
Same Product Code
19
Applicant Total
12
Review Days
62

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Basic Information

Device Name
CYSTOTOME, 140-S
K Number
K840475
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cilco, Inc.
Date Received
February 3, 1984
Decision Date
April 5, 1984
Product Code
HNY
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HNY Cystotome

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K844249 K-SOL
K843319 CILCO I/A SURGICAL PACK
K843992 CILCOR OPHTHALMIC INSTRUMENTS
K843447 CILCO DIAMOND KNIFE
K841099 OCTOPUS 500/500E
K832405 OPTHALMIC ENDOSCOPE
K827371 CILCO ASCAN
K820933 CILCO I/A HANDPIECE
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