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FDA 510(k)

PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE

K-Number: K925631 · 1993-07-29

ApplicantChiron Intraoptics
Decision Date1993-07-29
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Intraoptics. It received FDA 510(k) clearance on 1993-07-29 under 510(k) number K925631. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE?

PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE is a medical device that received FDA 510(k) clearance on 1993-07-29. The listed applicant is Chiron Intraoptics. The 510(k) number is K925631.

When did PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE receive FDA 510(k) clearance?

PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE received FDA 510(k) clearance on 1993-07-29, under 510(k) number K925631.

Who is the listed applicant for PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE?

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

What is the FDA product code for PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE?

The FDA product code for PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE is HQC.

Related Clinical Trials

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Other records listing Chiron Intraoptics 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.

K924165OPTISOL-GS CORNEAL STORAGE MEDIAK921729OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIEDK921728DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED

Related Devices (Code: HQC)

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.

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Official Source

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

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