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FDA 510(k)

PHILIPS VIEWFORUM 2003

K-Number: K032096 · 2003-07-18

ApplicantPhilips Medical Systems
Decision Date2003-07-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS VIEWFORUM 2003 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 2003-07-18 under 510(k) number K032096. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS VIEWFORUM 2003?

PHILIPS VIEWFORUM 2003 is a medical device that received FDA 510(k) clearance on 2003-07-18. The listed applicant is Philips Medical Systems. The 510(k) number is K032096.

When did PHILIPS VIEWFORUM 2003 receive FDA 510(k) clearance?

PHILIPS VIEWFORUM 2003 received FDA 510(k) clearance on 2003-07-18, under 510(k) number K032096.

Who is the listed applicant for PHILIPS VIEWFORUM 2003?

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 VIEWFORUM 2003?

The FDA product code for PHILIPS VIEWFORUM 2003 is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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