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FDA 510(k)

SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36

K-Number: K991503 · 1999-07-28

Decision Date1999-07-28
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 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 1999-07-28 under 510(k) number K991503. 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 SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36?

SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 is a medical device that received FDA 510(k) clearance on 1999-07-28. The listed applicant is United Pacific Co., Ltd.. The 510(k) number is K991503.

When did SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 receive FDA 510(k) clearance?

SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 received FDA 510(k) clearance on 1999-07-28, under 510(k) number K991503.

Who is the listed applicant for SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36?

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 SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36?

The FDA product code for SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 is ILY.

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 United Pacific Co., Ltd. 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: ILY)

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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