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FDA 510(k)

Image Management V15

K-Number: K240822 · 2024-04-24

Decision Date2024-04-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Image Management V15 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Technologies. It received FDA 510(k) clearance on 2024-04-24 under 510(k) number K240822. 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 Image Management V15?

Image Management V15 is a medical device that received FDA 510(k) clearance on 2024-04-24. The listed applicant is Philips Medical Systems Technologies. The 510(k) number is K240822.

When did Image Management V15 receive FDA 510(k) clearance?

Image Management V15 received FDA 510(k) clearance on 2024-04-24, under 510(k) number K240822.

Who is the listed applicant for Image Management V15?

The FDA 510(k) record lists Philips Medical Systems Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Image Management V15?

The FDA product code for Image Management V15 is LLZ.

Other records listing Philips Medical Systems Technologies 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.

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.

Official Source

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