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FDA 510(k)

Q-STATION

K-Number: K103815 · 2011-01-25

ApplicantPhilips Ultrasound, Inc.
Decision Date2011-01-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Q-STATION is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2011-01-25 under 510(k) number K103815. 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 Q-STATION?

Q-STATION is a medical device that received FDA 510(k) clearance on 2011-01-25. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K103815.

When did Q-STATION receive FDA 510(k) clearance?

Q-STATION received FDA 510(k) clearance on 2011-01-25, under 510(k) number K103815.

Who is the listed applicant for Q-STATION?

The FDA 510(k) record lists Philips Ultrasound, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-STATION?

The FDA product code for Q-STATION is LLZ.

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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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