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FDA 510(k)

BENJAMIN ENVOY PHACO HANDPIECE

K-Number: K022833 · 2002-09-09

Decision Date2002-09-09
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BENJAMIN ENVOY PHACO HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Benjamin Biomedical, Inc.. It received FDA 510(k) clearance on 2002-09-09 under 510(k) number K022833. 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 BENJAMIN ENVOY PHACO HANDPIECE?

BENJAMIN ENVOY PHACO HANDPIECE is a medical device that received FDA 510(k) clearance on 2002-09-09. The listed applicant is Benjamin Biomedical, Inc.. The 510(k) number is K022833.

When did BENJAMIN ENVOY PHACO HANDPIECE receive FDA 510(k) clearance?

BENJAMIN ENVOY PHACO HANDPIECE received FDA 510(k) clearance on 2002-09-09, under 510(k) number K022833.

Who is the listed applicant for BENJAMIN ENVOY PHACO HANDPIECE?

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

What is the FDA product code for BENJAMIN ENVOY PHACO HANDPIECE?

The FDA product code for BENJAMIN ENVOY PHACO HANDPIECE is HQC.

Related Clinical Trials

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.

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.

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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