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FDA 510(k)

MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921

K-Number: K071564 · 2007-08-31

ApplicantPhilips Medical Systems
Decision Date2007-08-31
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 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 2007-08-31 under 510(k) number K071564. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921?

MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 is a medical device that received FDA 510(k) clearance on 2007-08-31. The listed applicant is Philips Medical Systems. The 510(k) number is K071564.

When did MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 receive FDA 510(k) clearance?

MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 received FDA 510(k) clearance on 2007-08-31, under 510(k) number K071564.

Who is the listed applicant for MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921?

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 MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921?

The FDA product code for MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921 is DRG.

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Related Devices (Code: DRG)

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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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