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FDA 510(k)

CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW

K-Number: K993761 · 1999-12-28

ApplicantMedis Medical Imaging Systems BV
Decision Date1999-12-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Medis Medical Imaging Systems BV. It received FDA 510(k) clearance on 1999-12-28 under 510(k) number K993761. 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 CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW?

CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW is a medical device that received FDA 510(k) clearance on 1999-12-28. The listed applicant is Medis Medical Imaging Systems BV. The 510(k) number is K993761.

When did CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW receive FDA 510(k) clearance?

CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW received FDA 510(k) clearance on 1999-12-28, under 510(k) number K993761.

Who is the listed applicant for CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW?

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

What is the FDA product code for CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW?

The FDA product code for CARDIOVASCULAR MEASUREMENT SYSTEM - VIEW is LLZ.

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Other records listing Medis Medical Imaging Systems BV 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.

K182611Qangio XA 3DK112807X-RAY VVAK073156QPLAQUE MRK062386QANGIO CTK050703QBRAINK042383RSA-CMS

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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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