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FDA 510(k)

MODIFIED SITE FIBER OPTIC MODULE

K-Number: K924198 · 1992-11-23

ApplicantChiron Vision Corp.
Decision Date1992-11-23
Product CodeFCT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODIFIED SITE FIBER OPTIC MODULE 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 1992-11-23 under 510(k) number K924198. The device is classified under product code FCT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SITE FIBER OPTIC MODULE?

MODIFIED SITE FIBER OPTIC MODULE is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Chiron Vision Corp.. The 510(k) number is K924198.

When did MODIFIED SITE FIBER OPTIC MODULE receive FDA 510(k) clearance?

MODIFIED SITE FIBER OPTIC MODULE received FDA 510(k) clearance on 1992-11-23, under 510(k) number K924198.

Who is the listed applicant for MODIFIED SITE FIBER OPTIC MODULE?

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 FIBER OPTIC MODULE?

The FDA product code for MODIFIED SITE FIBER OPTIC MODULE is FCT.

Related Clinical Trials

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Other records listing Chiron Vision Corp. as applicant

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.

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: FCT)

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.

K960767LIGHT COMMANDERScieran Technologies, Inc.K883480MODIFIED SITE FIBER OPTIC MODULE FOR OPHTHAL. USESite Microsurgical Systems, Inc.K802769FIBER OPTIC HEADLIGHT #60-0765Aspen Laboratories, Inc.K802770FIBER OPTIC HEADLIGHT #60-0766766Aspen Laboratories, Inc.K780433FIBER OPTIC ADJUSTABLE HEADLIGHTCameron-Miller, Inc.

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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