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FDA 510(k)

STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE

K-Number: K926512 · 1993-09-09

ApplicantStorz
Decision Date1993-09-09
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Storz. It received FDA 510(k) clearance on 1993-09-09 under 510(k) number K926512. 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 STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE?

STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Storz. The 510(k) number is K926512.

When did STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE receive FDA 510(k) clearance?

STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE received FDA 510(k) clearance on 1993-09-09, under 510(k) number K926512.

Who is the listed applicant for STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE?

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

What is the FDA product code for STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE?

The FDA product code for STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE 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.

Other records listing Storz as applicant

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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