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FDA 510(k)

PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441

K-Number: K091176 · 2009-11-13

Decision Date2009-11-13
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441 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 2009-11-13 under 510(k) number K091176. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441?

PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441 is a medical device that received FDA 510(k) clearance on 2009-11-13. The listed applicant is Philips Medical Systems. The 510(k) number is K091176.

When did PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441 receive FDA 510(k) clearance?

PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441 received FDA 510(k) clearance on 2009-11-13, under 510(k) number K091176.

Who is the listed applicant for PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441?

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 TELEMEDICINE SERVER/SYSTEM, MODEL 861441?

The FDA product code for PHILIPS TELEMEDICINE SERVER/SYSTEM, MODEL 861441 is MSX.

Related Clinical Trials

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.

Other records listing Philips Medical Systems as applicant

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.

View all 99 devices →

Related Devices (Code: MSX)

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.

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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