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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2020-09-20 under 510(k) 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. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K200603.

When did AAA Model receive FDA 510(k) clearance?

AAA Model received FDA 510(k) clearance on 2020-09-20, under 510(k) number K200603.

Who is the listed applicant for AAA Model?

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 AAA Model?

The FDA product code for AAA Model is LLZ.

Other records listing Philips Ultrasound, Inc. as applicant

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Related Devices (Code: LLZ)

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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