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FDA 510(k)

VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS

K-Number: K883201 · 1988-09-26

ApplicantVital Metrics, Inc.
Decision Date1988-09-26
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS is the device name listed in this FDA 510(k) record. The listed applicant is Vital Metrics, Inc.. It received FDA 510(k) clearance on 1988-09-26 under 510(k) number K883201. The device is classified under product code HBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS?

VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS is a medical device that received FDA 510(k) clearance on 1988-09-26. The listed applicant is Vital Metrics, Inc.. The 510(k) number is K883201.

When did VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS receive FDA 510(k) clearance?

VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS received FDA 510(k) clearance on 1988-09-26, under 510(k) number K883201.

Who is the listed applicant for VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS?

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

What is the FDA product code for VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS?

The FDA product code for VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS is HBI.

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Other records listing Vital Metrics, 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.

K882956VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATIONK844973IRRIGA SUC ILLUM ISIS 710 & 7100 SERIESK843442URINARY DRAINAGE CONTAINER 2013 WITHK843441URINARY DRAINAGE CONTAINER 2012-WITHK840917URINARY MONITORING SYS 240K834448URINARY DRAINAGE CONTAINER

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Related Devices (Code: HBI)

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.

K223183Light-Guide CablesOlympus Winter & Ibe GmbHK163185OptiLux LED IlluminatorIsolux, LLCK111342LIGHT GUIDE CABLESchott North AmericaK0529791125 XSB XENON FIBER-OPTIC LIGHT SOURCEIsolux, LLCK021931ENDOSCOPIC FIBEROPTIC CABLEGulf Medical FiberopticsK991208ENDOSCOPIC FIBEROPTIC CABLEIsolux America

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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