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FDA 510(k)

HL888RA

K-Number: K031835 · 2003-07-01

ApplicantHealth & Life Co., Ltd.
Decision Date2003-07-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HL888RA is the device name listed in this FDA 510(k) record. The listed applicant is Health & Life Co., Ltd.. It received FDA 510(k) clearance on 2003-07-01 under 510(k) number K031835. 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 HL888RA?

HL888RA is a medical device that received FDA 510(k) clearance on 2003-07-01. The listed applicant is Health & Life Co., Ltd.. The 510(k) number is K031835.

When did HL888RA receive FDA 510(k) clearance?

HL888RA received FDA 510(k) clearance on 2003-07-01, under 510(k) number K031835.

Who is the listed applicant for HL888RA?

The FDA 510(k) record lists Health & Life Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HL888RA?

The FDA product code for HL888RA is DXN.

Other records listing Health & Life Co., Ltd. as applicant

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Related Devices (Code: DXN)

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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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