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FDA 510(k)

MODIFIED SITE POWER HANDPIECE II

K-Number: K932600 · 1994-01-25

ApplicantChiron Vision Corp.
Decision Date1994-01-25
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODIFIED SITE POWER HANDPIECE II is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K932600. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SITE POWER HANDPIECE II?

MODIFIED SITE POWER HANDPIECE II is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Chiron Vision Corp.. The 510(k) number is K932600.

When did MODIFIED SITE POWER HANDPIECE II receive FDA 510(k) clearance?

MODIFIED SITE POWER HANDPIECE II received FDA 510(k) clearance on 1994-01-25, under 510(k) number K932600.

Who is the listed applicant for MODIFIED SITE POWER HANDPIECE II?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED SITE POWER HANDPIECE II?

The FDA product code for MODIFIED SITE POWER HANDPIECE II is EKX.

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Other records listing Chiron Vision Corp. as applicant

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K970727MPORT FOLDABLE LENS PLACEMENT SYSTEMK972808HANSATOME MICROKERATOMEK960414SYNERGIST POWER PACKK944993IOLAB.SITE CD PHACOEMULSIFICATION MODULEK944995IOLAB/SITE PERISTALTIC MODULEK951292PASSPORT FOLDABLE LENS PLACEMENT SYSTEM

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Related Devices (Code: EKX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261987Reusable SmartPegOsstell ABK252223Alpha Endo Handpiece (Alpha Endo)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K251597InnerView SystemPerimetrics, Inc.K243692EnDrive (EnDriveUS)Advanced Technology Research (A.T.R.) S.R.L.K242514Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)Shenzhen Rogin Medical Co., Ltd.K241065ChecQ (AC100)Dentis Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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