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FDA 510(k)

AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM

K-Number: K011779 · 2001-07-13

Decision Date2001-07-13
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Avid Care Corp.. It received FDA 510(k) clearance on 2001-07-13 under 510(k) number K011779. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM?

AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2001-07-13. The listed applicant is Avid Care Corp.. The 510(k) number is K011779.

When did AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM receive FDA 510(k) clearance?

AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM received FDA 510(k) clearance on 2001-07-13, under 510(k) number K011779.

Who is the listed applicant for AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM?

The FDA 510(k) record lists Avid Care Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM?

The FDA product code for AVIDCARE SERIES 100 TELEMANAGEMENT SYSTEM is DXN.

Related Clinical Trials

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.

Other records listing Avid Care Corp. 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: DXN)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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