Compression Therapy Device
K-Number: K191856 · 2020-03-19
Device Summary
Frequently Asked Questions
What is the Compression Therapy Device?
Compression Therapy Device is a medical device that received FDA 510(k) clearance on 2020-03-19. The listed applicant is Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K191856.
When did Compression Therapy Device receive FDA 510(k) clearance?
Compression Therapy Device received FDA 510(k) clearance on 2020-03-19, under 510(k) number K191856.
Who is the listed applicant for Compression Therapy Device?
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?
The FDA product code for Compression Therapy Device is JOW.
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: JOW)
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.