FDA 510(k)

IOLAB.SITE CD PHACOEMULSIFICATION MODULE

K-Number: K944993 · 1995-10-12

Decision Date1995-10-12

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

IOLAB.SITE CD PHACOEMULSIFICATION 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 1995-10-12 under 510(k) number K944993. 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 IOLAB.SITE CD PHACOEMULSIFICATION MODULE?

IOLAB.SITE CD PHACOEMULSIFICATION MODULE is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is Chiron Vision Corp.. The 510(k) number is K944993.

When did IOLAB.SITE CD PHACOEMULSIFICATION MODULE receive FDA 510(k) clearance?

IOLAB.SITE CD PHACOEMULSIFICATION MODULE received FDA 510(k) clearance on 1995-10-12, under 510(k) number K944993.

Who is the listed applicant for IOLAB.SITE CD PHACOEMULSIFICATION 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 IOLAB.SITE CD PHACOEMULSIFICATION MODULE?

The FDA product code for IOLAB.SITE CD PHACOEMULSIFICATION MODULE is HQC.

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Other records listing Chiron Vision Corp. as applicant

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Related Devices (Code: HQC)

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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.