AAA Model
K-Number: K200603 · 2020-09-20
ApplicantPhilips Ultrasound, Inc.
Decision Date2020-09-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AAA Model is a medical device manufactured by Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2020-09-20 under approval number K200603. 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 AAA Model?
AAA Model is a medical device that received FDA 510(k) clearance on 2020-09-20. It is manufactured by Philips Ultrasound, Inc.. The 510(k) number is K200603.
When was AAA Model approved by the FDA?
AAA Model received FDA 510(k) clearance on 2020-09-20, under approval number K200603.
What company makes AAA Model?
AAA Model is manufactured by Philips Ultrasound, Inc..
What is the FDA product code for AAA Model?
The FDA product code for AAA Model is LLZ.
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Related Devices (Code: LLZ)
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.