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FDA 510(k)

PRACTIX CONVENIO

K-Number: K042368 · 2004-10-04

ApplicantPhilips Medical Systems North America Co.
Decision Date2004-10-04
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRACTIX CONVENIO is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America Co.. It received FDA 510(k) clearance on 2004-10-04 under 510(k) number K042368. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRACTIX CONVENIO?

PRACTIX CONVENIO is a medical device that received FDA 510(k) clearance on 2004-10-04. The listed applicant is Philips Medical Systems North America Co.. The 510(k) number is K042368.

When did PRACTIX CONVENIO receive FDA 510(k) clearance?

PRACTIX CONVENIO received FDA 510(k) clearance on 2004-10-04, under 510(k) number K042368.

Who is the listed applicant for PRACTIX CONVENIO?

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

What is the FDA product code for PRACTIX CONVENIO?

The FDA product code for PRACTIX CONVENIO is IZL.

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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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