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FDA 510(k)

VARIS PORTALVISION

K-Number: K955774 · 1996-03-15

ApplicantVarian Assoc., Inc.
Decision Date1996-03-15
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIS PORTALVISION is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K955774. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIS PORTALVISION?

VARIS PORTALVISION is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K955774.

When did VARIS PORTALVISION receive FDA 510(k) clearance?

VARIS PORTALVISION received FDA 510(k) clearance on 1996-03-15, under 510(k) number K955774.

Who is the listed applicant for VARIS PORTALVISION?

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

What is the FDA product code for VARIS PORTALVISION?

The FDA product code for VARIS PORTALVISION is IYE.

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Other records listing Varian Assoc., 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.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

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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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