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

CILCO DIAMOND KNIFE

K Number: K843447 · Decision Oct 5, 1984
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
53
Applicant Total
12
Review Days
30

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Basic Information

Device Name
CILCO DIAMOND KNIFE
K Number
K843447
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cilco, Inc.
Date Received
September 5, 1984
Decision Date
October 5, 1984
Product Code
HNN
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
HNN Knife, Ophthalmic

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Other Clearances by Cilco, Inc.

K Number Device Name
K861334 CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE
K854969 CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)
K844249 K-SOL
K843319 CILCO I/A SURGICAL PACK
K843992 CILCOR OPHTHALMIC INSTRUMENTS
K841099 OCTOPUS 500/500E
K840475 CYSTOTOME, 140-S
K832405 OPTHALMIC ENDOSCOPE
K827371 CILCO ASCAN
K820933 CILCO I/A HANDPIECE
Search all 12 clearances from Cilco, Inc. →