FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

IOLAB LACRIMAL DUCT CATHETER

K Number: K935233 · Decision Sep 15, 1994
Classifications
1
FEI Numbers
20
Registration Numbers
21
Same Product Code
30
Applicant Total
34
Review Days
318

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Basic Information

Device Name
IOLAB LACRIMAL DUCT CATHETER
K Number
K935233
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Vision Corp.
Date Received
November 1, 1993
Decision Date
September 15, 1994
Product Code
OKS
Advisory Committee
Unknown
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
OKS Lacrimal Stents And Intubation Sets

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Other Clearances by Chiron Vision Corp.

K Number Device Name
K970727 MPORT FOLDABLE LENS PLACEMENT SYSTEM
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
K925606 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
K926412 MICRON-SCOPE II
Search all 34 clearances from Chiron Vision Corp. →