FDA 510(k)

COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM

K-Number: K083413 · 2008-12-18

Decision Date2008-12-18

Product CodeBSZ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM 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 2008-12-18 under 510(k) number K083413. 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 COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM?

COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM is a medical device that received FDA 510(k) clearance on 2008-12-18. The listed applicant is Philips Medical Systems. The 510(k) number is K083413.

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

COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM received FDA 510(k) clearance on 2008-12-18, under 510(k) number K083413.

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

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 COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM?

The FDA product code for COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM 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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Related Devices (Code: BSZ)

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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.