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FDA 510(k)

GAUNYING INFRARED LAMP MODEL IL50

K-Number: K101693 · 2011-01-05

Decision Date2011-01-05
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GAUNYING INFRARED LAMP MODEL IL50 is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Gaunying Electronics Co., Ltd.. It received FDA 510(k) clearance on 2011-01-05 under 510(k) number K101693. 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 GAUNYING INFRARED LAMP MODEL IL50?

GAUNYING INFRARED LAMP MODEL IL50 is a medical device that received FDA 510(k) clearance on 2011-01-05. The listed applicant is Foshan Gaunying Electronics Co., Ltd.. The 510(k) number is K101693.

When did GAUNYING INFRARED LAMP MODEL IL50 receive FDA 510(k) clearance?

GAUNYING INFRARED LAMP MODEL IL50 received FDA 510(k) clearance on 2011-01-05, under 510(k) number K101693.

Who is the listed applicant for GAUNYING INFRARED LAMP MODEL IL50?

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

What is the FDA product code for GAUNYING INFRARED LAMP MODEL IL50?

The FDA product code for GAUNYING INFRARED LAMP MODEL IL50 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 Foshan Gaunying Electronics 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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