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

CILCO I/A HANDPIECE

K Number: K820933 · Decision Jun 14, 1982
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
12
Review Days
73

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Basic Information

Device Name
CILCO I/A HANDPIECE
K Number
K820933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cilco, Inc.
Date Received
April 2, 1982
Decision Date
June 14, 1982
Product Code
HQE
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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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
K843447 CILCO DIAMOND KNIFE
K841099 OCTOPUS 500/500E
K840475 CYSTOTOME, 140-S
K832405 OPTHALMIC ENDOSCOPE
K827371 CILCO ASCAN
Search all 12 clearances from Cilco, Inc. →