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FDA 510(k)

MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS

K-Number: K922996 · 1992-07-27

ApplicantChiron Vision Corp.
Decision Date1992-07-27
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS 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 1992-07-27 under 510(k) number K922996. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS?

MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS is a medical device that received FDA 510(k) clearance on 1992-07-27. The listed applicant is Chiron Vision Corp.. The 510(k) number is K922996.

When did MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS receive FDA 510(k) clearance?

MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS received FDA 510(k) clearance on 1992-07-27, under 510(k) number K922996.

Who is the listed applicant for MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS?

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 DIAPHRAGM CASSETTE FOR OPHTHALMICS?

The FDA product code for MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS is KYG.

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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: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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