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FDA 510(k)

ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.

K-Number: K052562 · 2005-12-23

Decision Date2005-12-23
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS. is the device name listed in this FDA 510(k) record. The listed applicant is Interacoustics AS. It received FDA 510(k) clearance on 2005-12-23 under 510(k) number K052562. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.?

ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS. is a medical device that received FDA 510(k) clearance on 2005-12-23. The listed applicant is Interacoustics AS. The 510(k) number is K052562.

When did ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS. receive FDA 510(k) clearance?

ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS. received FDA 510(k) clearance on 2005-12-23, under 510(k) number K052562.

Who is the listed applicant for ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.?

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

What is the FDA product code for ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.?

The FDA product code for ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS. is EWO.

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 Interacoustics AS 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: EWO)

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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