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FDA 510(k)

PHACOSCOPE

K-Number: K960811 · 1996-10-02

ApplicantSaint John'S Plaza Medical Group
Decision Date1996-10-02
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Saint John'S Plaza Medical Group. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K960811. 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 PHACOSCOPE?

PHACOSCOPE is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Saint John'S Plaza Medical Group. The 510(k) number is K960811.

When did PHACOSCOPE receive FDA 510(k) clearance?

PHACOSCOPE received FDA 510(k) clearance on 1996-10-02, under 510(k) number K960811.

Who is the listed applicant for PHACOSCOPE?

The FDA 510(k) record lists Saint John'S Plaza Medical Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHACOSCOPE?

The FDA product code for PHACOSCOPE is HQC.

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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.

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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.

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