Compression Therapy Device Model LGT-2200SP
K-Number: K191862 · 2019-10-29
Device Summary
Frequently Asked Questions
What is the Compression Therapy Device Model LGT-2200SP?
Compression Therapy Device Model LGT-2200SP is a medical device that received FDA 510(k) clearance on 2019-10-29. The listed applicant is Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K191862.
When did Compression Therapy Device Model LGT-2200SP receive FDA 510(k) clearance?
Compression Therapy Device Model LGT-2200SP received FDA 510(k) clearance on 2019-10-29, under 510(k) number K191862.
Who is the listed applicant for Compression Therapy Device Model LGT-2200SP?
The FDA 510(k) record lists Guangzhou Longest Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compression Therapy Device Model LGT-2200SP?
The FDA product code for Compression Therapy Device Model LGT-2200SP is IRP.
Other records listing Guangzhou Longest Science & Technology 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: IRP)
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.