Overlapped Compression Therapy
K-Number: K202839 · 2021-01-21
Device Summary
Frequently Asked Questions
What is the Overlapped Compression Therapy?
Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2021-01-21. The listed applicant is Jkh Health Co., Ltd.. The 510(k) number is K202839.
When did Overlapped Compression Therapy receive FDA 510(k) clearance?
Overlapped Compression Therapy received FDA 510(k) clearance on 2021-01-21, under 510(k) number K202839.
Who is the listed applicant for Overlapped Compression Therapy?
The FDA 510(k) record lists Jkh Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Overlapped Compression Therapy?
The FDA product code for Overlapped Compression Therapy is JOW.
Other records listing Jkh Health 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.