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

SITE ANTERIOR CAPSULOTOMER

K Number: K843039 · Decision Nov 21, 1984
Classifications
1
FEI Numbers
234
Registration Numbers
235
Same Product Code
76
Applicant Total
34
Review Days
111

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Basic Information

Device Name
SITE ANTERIOR CAPSULOTOMER
K Number
K843039
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Chiron Vision Corp.
Date Received
August 2, 1984
Decision Date
November 21, 1984
Product Code
HMX
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
HMX Cannula, Ophthalmic

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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
K935233 IOLAB LACRIMAL DUCT CATHETER
K925606 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
Search all 34 clearances from Chiron Vision Corp. →