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FDA 510(k)

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02

K-Number: K021422 · 2002-05-15

ApplicantPhilips Medical Systems
Decision Date2002-05-15
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2002-05-15 under 510(k) number K021422. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02?

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 is a medical device that received FDA 510(k) clearance on 2002-05-15. The listed applicant is Philips Medical Systems. The 510(k) number is K021422.

When did PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 receive FDA 510(k) clearance?

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 received FDA 510(k) clearance on 2002-05-15, under 510(k) number K021422.

Who is the listed applicant for PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02?

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

What is the FDA product code for PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02?

The FDA product code for PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 is MHX.

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Other records listing Philips Medical Systems as applicant

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K212704Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound SystemK211597EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound SystemK210560Page Writer TC20 Cardiograph, Page Writer TC30 Cardiograph, Page Writer TC50 Cardiograph, Page Writer TC70 CardiographK191738PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 CardiographK192875Philips Biosensor BX100K183387M3290B Patient Information Center iX

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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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