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

MICRON-SCOPE II

K Number: K926412 · Decision Jul 19, 1994
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
34
Review Days
575

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Basic Information

Device Name
MICRON-SCOPE II
K Number
K926412
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4230
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Chiron Vision Corp.
Date Received
December 21, 1992
Decision Date
July 19, 1994
Product Code
HMS
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
HMS Drum, Eye Knife Test

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K951292 PASSPORT FOLDABLE LENS PLACEMENT SYSTEM
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K941550 AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
K935233 IOLAB LACRIMAL DUCT CATHETER
K925606 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
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