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FDA 510(k)

EVOLUTION PHACOMULSIFIER

K-Number: K954240 · 1995-12-01

ApplicantU.S. Iol, Inc.
Decision Date1995-12-01
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EVOLUTION PHACOMULSIFIER is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Iol, Inc.. It received FDA 510(k) clearance on 1995-12-01 under 510(k) number K954240. 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 EVOLUTION PHACOMULSIFIER?

EVOLUTION PHACOMULSIFIER is a medical device that received FDA 510(k) clearance on 1995-12-01. The listed applicant is U.S. Iol, Inc.. The 510(k) number is K954240.

When did EVOLUTION PHACOMULSIFIER receive FDA 510(k) clearance?

EVOLUTION PHACOMULSIFIER received FDA 510(k) clearance on 1995-12-01, under 510(k) number K954240.

Who is the listed applicant for EVOLUTION PHACOMULSIFIER?

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

What is the FDA product code for EVOLUTION PHACOMULSIFIER?

The FDA product code for EVOLUTION PHACOMULSIFIER 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.

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Other records listing U.S. Iol, 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.

K001768OCCU-FLO PUNCTUM PLUGSK954746PHACO TIPK954239U.S. IOL PHACO HANDPIECE

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.

K261264Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+Bausch and LombK252052Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)Bausch and Lomb, IncorporatedK250501System SophiThis AGK243395MICOR 700 with Auto I/ACarl Zeiss Meditec Cataract Technology, Inc.K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)Carl Zeiss Meditec Cataract Technology, Inc.K240169Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)Bausch and Lomb, Incorporated

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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