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FDA 510(k)

VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM

K-Number: K900064 · 1990-03-09

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1990-03-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K900064. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM?

VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K900064.

When did VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM receive FDA 510(k) clearance?

VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900064.

Who is the listed applicant for VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM?

The FDA product code for VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM is LNH.

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Official Source

View on FDA Database →

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