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

MODIFIED SITE POWER HANDPIECE

K Number: K922077 · Decision Jun 23, 1992
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
34
Review Days
50

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Basic Information

Device Name
MODIFIED SITE POWER HANDPIECE
K Number
K922077
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Vision Corp.
Date Received
May 4, 1992
Decision Date
June 23, 1992
Product Code
EKX
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EKX Handpiece, Direct Drive, Ac-Powered

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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. →