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FDA 510(k)

MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM

K-Number: K883199 · 1988-09-15

ApplicantChiron Vision Corp.
Decision Date1988-09-15
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM 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 1988-09-15 under 510(k) number K883199. 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 MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM?

MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is Chiron Vision Corp.. The 510(k) number is K883199.

When did MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM received FDA 510(k) clearance on 1988-09-15, under 510(k) number K883199.

Who is the listed applicant for MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM?

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 MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM?

The FDA product code for MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM is HQC.

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Other records listing Chiron Vision Corp. as applicant

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K970727MPORT FOLDABLE LENS PLACEMENT SYSTEMK972808HANSATOME MICROKERATOMEK960414SYNERGIST POWER PACKK944993IOLAB.SITE CD PHACOEMULSIFICATION MODULEK944995IOLAB/SITE PERISTALTIC MODULEK951292PASSPORT FOLDABLE LENS PLACEMENT SYSTEM

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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.

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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