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FDA 510(k)

IOCARE CONVERTER KIT

K-Number: K843276 · 1985-05-09

ApplicantChiron Vision Corp.
Decision Date1985-05-09
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IOCARE CONVERTER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1985-05-09 under 510(k) number K843276. 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 IOCARE CONVERTER KIT?

IOCARE CONVERTER KIT is a medical device that received FDA 510(k) clearance on 1985-05-09. The listed applicant is Chiron Vision Corp.. The 510(k) number is K843276.

When did IOCARE CONVERTER KIT receive FDA 510(k) clearance?

IOCARE CONVERTER KIT received FDA 510(k) clearance on 1985-05-09, under 510(k) number K843276.

Who is the listed applicant for IOCARE CONVERTER KIT?

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

What is the FDA product code for IOCARE CONVERTER KIT?

The FDA product code for IOCARE CONVERTER KIT is HQC.

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Related Devices (Code: HQC)

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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

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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