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

CONSTELLATION VISION SYSTEM

K Number: K141065 · Decision Aug 22, 2014
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
16
Review Days
120

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Basic Information

Device Name
CONSTELLATION VISION SYSTEM
K Number
K141065
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alcon Research, Ltd.
Date Received
April 24, 2014
Decision Date
August 22, 2014
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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K110951 27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA
K110166 CLEARCUT S SAFETY KNIFE
K102860 ALCON MULTI-PIRPOSE DISINFECTING SOLUTION
K101006 WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
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