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FDA 510(k)

PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM

K-Number: K955268 · 1996-01-30

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1996-01-30
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PQ-2000+ COMPUTED TOMOGRAPHY X-RAY 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 1996-01-30 under 510(k) number K955268. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM?

PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K955268.

When did PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM receive FDA 510(k) clearance?

PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955268.

Who is the listed applicant for PQ-2000+ COMPUTED TOMOGRAPHY X-RAY 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 PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM?

The FDA product code for PQ-2000+ COMPUTED TOMOGRAPHY X-RAY SYSTEM is JAK.

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Related Devices (Code: JAK)

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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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