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FDA 510(k)

PHACO NEEDLES AND TIPS

K-Number: K943672 · 1994-10-13

Decision Date1994-10-13
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACO NEEDLES AND TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Microsurgical Technology, Inc.. It received FDA 510(k) clearance on 1994-10-13 under 510(k) number K943672. 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 PHACO NEEDLES AND TIPS?

PHACO NEEDLES AND TIPS is a medical device that received FDA 510(k) clearance on 1994-10-13. The listed applicant is Microsurgical Technology, Inc.. The 510(k) number is K943672.

When did PHACO NEEDLES AND TIPS receive FDA 510(k) clearance?

PHACO NEEDLES AND TIPS received FDA 510(k) clearance on 1994-10-13, under 510(k) number K943672.

Who is the listed applicant for PHACO NEEDLES AND TIPS?

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

What is the FDA product code for PHACO NEEDLES AND TIPS?

The FDA product code for PHACO NEEDLES AND TIPS 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 Microsurgical Technology, Inc. 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.

View all 9 devices →

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

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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