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

MPORT FOLDABLE LENS PLACEMENT SYSTEM

K Number: K970727 · Decision Dec 17, 1997
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
62
Applicant Total
34
Review Days
292

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Basic Information

Device Name
MPORT FOLDABLE LENS PLACEMENT SYSTEM
K Number
K970727
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Vision Corp.
Date Received
February 28, 1997
Decision Date
December 17, 1997
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)

Similar 510(k) Clearances

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Other Clearances by Chiron Vision Corp.

K Number Device Name
K972808 HANSATOME MICROKERATOME
K960414 SYNERGIST POWER PACK
K944993 IOLAB.SITE CD PHACOEMULSIFICATION MODULE
K944995 IOLAB/SITE PERISTALTIC MODULE
K951292 PASSPORT FOLDABLE LENS PLACEMENT SYSTEM
K944994 IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE
K941550 AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
K935233 IOLAB LACRIMAL DUCT CATHETER
K925606 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
K926412 MICRON-SCOPE II
Search all 34 clearances from Chiron Vision Corp. →