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FDA 510(k)

MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK

K-Number: K033941 · 2004-02-10

ApplicantBausch & Lomb, Inc.
Decision Date2004-02-10
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC 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 2004-02-10 under 510(k) number K033941. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK?

MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK is a medical device that received FDA 510(k) clearance on 2004-02-10. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K033941.

When did MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK receive FDA 510(k) clearance?

MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK received FDA 510(k) clearance on 2004-02-10, under 510(k) number K033941.

Who is the listed applicant for MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC 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 MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK?

The FDA product code for MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK is HQF.

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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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