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FDA 510(k)

OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS

K-Number: K925606 · 1994-08-29

ApplicantChiron Vision Corp.
Decision Date1994-08-29
Product CodeHMR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS 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 1994-08-29 under 510(k) number K925606. The device is classified under product code HMR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS?

OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS is a medical device that received FDA 510(k) clearance on 1994-08-29. The listed applicant is Chiron Vision Corp.. The 510(k) number is K925606.

When did OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS receive FDA 510(k) clearance?

OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS received FDA 510(k) clearance on 1994-08-29, under 510(k) number K925606.

Who is the listed applicant for OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS?

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 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS?

The FDA product code for OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS is HMR.

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Other records listing Chiron Vision Corp. as applicant

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Related Devices (Code: HMR)

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.

K053475OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450Refractec, Inc.K872747LASER CENTERING DEVICEInnomed Corp.K863663OPHTHALMIC SURGICAL OCULAR MARKERSMyocure, Inc.K861535OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNUCooperVision, 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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