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FDA 510(k)

M2376A PHILIPS DEVICE LINK SYSTEM

K-Number: K033680 · 2003-12-11

ApplicantPhilips Medical Systems
Decision Date2003-12-11
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M2376A PHILIPS DEVICE LINK 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 2003-12-11 under 510(k) number K033680. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M2376A PHILIPS DEVICE LINK SYSTEM?

M2376A PHILIPS DEVICE LINK SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-11. The listed applicant is Philips Medical Systems. The 510(k) number is K033680.

When did M2376A PHILIPS DEVICE LINK SYSTEM receive FDA 510(k) clearance?

M2376A PHILIPS DEVICE LINK SYSTEM received FDA 510(k) clearance on 2003-12-11, under 510(k) number K033680.

Who is the listed applicant for M2376A PHILIPS DEVICE LINK 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 M2376A PHILIPS DEVICE LINK SYSTEM?

The FDA product code for M2376A PHILIPS DEVICE LINK SYSTEM is MWI.

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Other records listing Philips Medical Systems as applicant

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Related Devices (Code: MWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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