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FDA 510(k)

AQUABOSS ECORO DIA 50

K-Number: K032004 · 2003-10-02

ApplicantLauer Ltd., Hong Kong
Decision Date2003-10-02
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AQUABOSS ECORO DIA 50 is the device name listed in this FDA 510(k) record. The listed applicant is Lauer Ltd., Hong Kong. It received FDA 510(k) clearance on 2003-10-02 under 510(k) number K032004. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUABOSS ECORO DIA 50?

AQUABOSS ECORO DIA 50 is a medical device that received FDA 510(k) clearance on 2003-10-02. The listed applicant is Lauer Ltd., Hong Kong. The 510(k) number is K032004.

When did AQUABOSS ECORO DIA 50 receive FDA 510(k) clearance?

AQUABOSS ECORO DIA 50 received FDA 510(k) clearance on 2003-10-02, under 510(k) number K032004.

Who is the listed applicant for AQUABOSS ECORO DIA 50?

The FDA 510(k) record lists Lauer Ltd., Hong Kong as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUABOSS ECORO DIA 50?

The FDA product code for AQUABOSS ECORO DIA 50 is FIP.

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Related Devices (Code: FIP)

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

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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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