GAUNYING INFRARED LAMP
K-Number: K102149 · 2010-08-13
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Device Summary
Frequently Asked Questions
What is the GAUNYING INFRARED LAMP?
GAUNYING INFRARED LAMP is a medical device that received FDA 510(k) clearance on 2010-08-13. The listed applicant is Foshan Gaunying Electronics Co., Ltd.. The 510(k) number is K102149.
When did GAUNYING INFRARED LAMP receive FDA 510(k) clearance?
GAUNYING INFRARED LAMP received FDA 510(k) clearance on 2010-08-13, under 510(k) number K102149.
Who is the listed applicant for GAUNYING INFRARED LAMP?
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?
The FDA product code for GAUNYING INFRARED LAMP 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
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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