FDA 510(k)

VENTURI PHACO PACK

K-Number: K033653 · 2003-12-17

Decision Date2003-12-17

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

VENTURI PHACO PACK is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2003-12-17 under 510(k) number K033653. 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 VENTURI PHACO PACK?

VENTURI PHACO PACK is a medical device that received FDA 510(k) clearance on 2003-12-17. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K033653.

When did VENTURI PHACO PACK receive FDA 510(k) clearance?

VENTURI PHACO PACK received FDA 510(k) clearance on 2003-12-17, under 510(k) number K033653.

Who is the listed applicant for VENTURI PHACO PACK?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTURI PHACO PACK?

The FDA product code for VENTURI PHACO PACK is HQC.

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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.