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FDA 510(k)

STAAR PHACO XL SMALL INCISION SYSTEM

K-Number: K884241 · 1989-02-17

Decision Date1989-02-17
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STAAR PHACO XL SMALL INCISION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Staar Surgical Co.. It received FDA 510(k) clearance on 1989-02-17 under 510(k) number K884241. 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 STAAR PHACO XL SMALL INCISION SYSTEM?

STAAR PHACO XL SMALL INCISION SYSTEM is a medical device that received FDA 510(k) clearance on 1989-02-17. The listed applicant is Staar Surgical Co.. The 510(k) number is K884241.

When did STAAR PHACO XL SMALL INCISION SYSTEM receive FDA 510(k) clearance?

STAAR PHACO XL SMALL INCISION SYSTEM received FDA 510(k) clearance on 1989-02-17, under 510(k) number K884241.

Who is the listed applicant for STAAR PHACO XL SMALL INCISION SYSTEM?

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

What is the FDA product code for STAAR PHACO XL SMALL INCISION SYSTEM?

The FDA product code for STAAR PHACO XL SMALL INCISION SYSTEM 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 Staar Surgical Co. 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 22 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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