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FDA 510(k)

CX250 MOBILE GAMMA CAMERA & DCS CONSOLE

K-Number: K880878 · 1988-09-01

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1988-09-01
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CX250 MOBILE GAMMA CAMERA & DCS CONSOLE 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 1988-09-01 under 510(k) number K880878. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CX250 MOBILE GAMMA CAMERA & DCS CONSOLE?

CX250 MOBILE GAMMA CAMERA & DCS CONSOLE is a medical device that received FDA 510(k) clearance on 1988-09-01. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K880878.

When did CX250 MOBILE GAMMA CAMERA & DCS CONSOLE receive FDA 510(k) clearance?

CX250 MOBILE GAMMA CAMERA & DCS CONSOLE received FDA 510(k) clearance on 1988-09-01, under 510(k) number K880878.

Who is the listed applicant for CX250 MOBILE GAMMA CAMERA & DCS CONSOLE?

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 CX250 MOBILE GAMMA CAMERA & DCS CONSOLE?

The FDA product code for CX250 MOBILE GAMMA CAMERA & DCS CONSOLE is IYX.

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Related Devices (Code: IYX)

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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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