FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER

K Number: K011392 · Decision Oct 22, 2001
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
62
Applicant Total
1
Review Days
168

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Basic Information

Device Name
MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER
K Number
K011392
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Micra Instruments
Date Received
May 7, 2001
Decision Date
October 22, 2001
Product Code
MSS
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
MSS Folders And Injectors, Intraocular Lens (Iol)

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