FDA 510(k)

PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE

K-Number: K030939 · 2003-07-15

Decision Date2003-07-15

Product CodeBSZ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE 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 2003-07-15 under 510(k) number K030939. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE?

PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE is a medical device that received FDA 510(k) clearance on 2003-07-15. The listed applicant is Philips Medical Systems. The 510(k) number is K030939.

When did PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE receive FDA 510(k) clearance?

PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE received FDA 510(k) clearance on 2003-07-15, under 510(k) number K030939.

Who is the listed applicant for PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE?

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 COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE?

The FDA product code for PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE is BSZ.

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Other records listing Philips Medical Systems as applicant

K212704Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System K211597EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System K210560Page Writer TC20 Cardiograph, Page Writer TC30 Cardiograph, Page Writer TC50 Cardiograph, Page Writer TC70 Cardiograph K191738PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 Cardiograph K192875Philips Biosensor BX100 K183387M3290B 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.