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FDA 510(k)

CAAS MRV VERSION 3.0

K-Number: K060941 · 2006-04-19

ApplicantPie Medical Imaging BV
Decision Date2006-04-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAAS MRV VERSION 3.0 is the device name listed in this FDA 510(k) record. The listed applicant is Pie Medical Imaging BV. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060941. 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 CAAS MRV VERSION 3.0?

CAAS MRV VERSION 3.0 is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Pie Medical Imaging BV. The 510(k) number is K060941.

When did CAAS MRV VERSION 3.0 receive FDA 510(k) clearance?

CAAS MRV VERSION 3.0 received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060941.

Who is the listed applicant for CAAS MRV VERSION 3.0?

The FDA 510(k) record lists Pie Medical Imaging BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAAS MRV VERSION 3.0?

The FDA product code for CAAS MRV VERSION 3.0 is LLZ.

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Other records listing Pie Medical Imaging BV 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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