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FDA 510(k)

CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM

K-Number: K020449 · 2002-05-10

ApplicantCardionow, Inc.
Decision Date2002-05-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cardionow, Inc.. It received FDA 510(k) clearance on 2002-05-10 under 510(k) number K020449. 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 CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM?

CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-05-10. The listed applicant is Cardionow, Inc.. The 510(k) number is K020449.

When did CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM receive FDA 510(k) clearance?

CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM received FDA 510(k) clearance on 2002-05-10, under 510(k) number K020449.

Who is the listed applicant for CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM?

The FDA 510(k) record lists Cardionow, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM?

The FDA product code for CARDIONOW CARDIOLOGY WIDE AREA ARCHIVE AND RETRIEVAL SYSTEM is LLZ.

Related Clinical Trials

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Other records listing Cardionow, Inc. 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.

K002597CN ACQUISITION STATION

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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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