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FDA 510(k)

VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION

K-Number: K882956 · 1988-08-03

ApplicantVital Metrics, Inc.
Decision Date1988-08-03
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION 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 1988-08-03 under 510(k) number K882956. 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 AND IRRIGATION?

VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is Vital Metrics, Inc.. The 510(k) number is K882956.

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

VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION received FDA 510(k) clearance on 1988-08-03, under 510(k) number K882956.

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

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 AND IRRIGATION?

The FDA product code for VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION 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.

K883201VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYSK844973IRRIGA 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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