FDA 510(k)

QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B

K-Number: K993123 · 1999-12-17

Decision Date1999-12-17

Product CodeILY

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B is the device name listed in this FDA 510(k) record. The listed applicant is United Pacific Co., Ltd.. It received FDA 510(k) clearance on 1999-12-17 under 510(k) number K993123. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B?

QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B is a medical device that received FDA 510(k) clearance on 1999-12-17. The listed applicant is United Pacific Co., Ltd.. The 510(k) number is K993123.

When did QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B receive FDA 510(k) clearance?

QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B received FDA 510(k) clearance on 1999-12-17, under 510(k) number K993123.

Who is the listed applicant for QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B?

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

What is the FDA product code for QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B?

The FDA product code for QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B is ILY.

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Related Devices (Code: ILY)

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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.