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FDA 510(k)

C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS

K-Number: K883521 · 1988-09-02

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1988-09-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS 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 1988-09-02 under 510(k) number K883521. 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 C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS?

C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS is a medical device that received FDA 510(k) clearance on 1988-09-02. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K883521.

When did C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS receive FDA 510(k) clearance?

C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS received FDA 510(k) clearance on 1988-09-02, under 510(k) number K883521.

Who is the listed applicant for C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS?

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 C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS?

The FDA product code for C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS is LNH.

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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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