FDA 510(k)

ALCON SERIES 20000 LEGACY PHACOEMULSIFIER

K-Number: K952213 · 1995-08-09

Decision Date1995-08-09

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

ALCON SERIES 20000 LEGACY PHACOEMULSIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1995-08-09 under 510(k) number K952213. 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 ALCON SERIES 20000 LEGACY PHACOEMULSIFIER?

ALCON SERIES 20000 LEGACY PHACOEMULSIFIER is a medical device that received FDA 510(k) clearance on 1995-08-09. The listed applicant is Alcon Laboratories. The 510(k) number is K952213.

When did ALCON SERIES 20000 LEGACY PHACOEMULSIFIER receive FDA 510(k) clearance?

ALCON SERIES 20000 LEGACY PHACOEMULSIFIER received FDA 510(k) clearance on 1995-08-09, under 510(k) number K952213.

Who is the listed applicant for ALCON SERIES 20000 LEGACY PHACOEMULSIFIER?

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

What is the FDA product code for ALCON SERIES 20000 LEGACY PHACOEMULSIFIER?

The FDA product code for ALCON SERIES 20000 LEGACY PHACOEMULSIFIER is 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.