Cold Compression Wrap Pro
K-Number: K230524 · 2024-01-19
Device Summary
Frequently Asked Questions
What is the Cold Compression Wrap Pro?
Cold Compression Wrap Pro is a medical device that received FDA 510(k) clearance on 2024-01-19. The listed applicant is Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K230524.
When did Cold Compression Wrap Pro receive FDA 510(k) clearance?
Cold Compression Wrap Pro received FDA 510(k) clearance on 2024-01-19, under 510(k) number K230524.
Who is the listed applicant for Cold Compression Wrap Pro?
The FDA 510(k) record lists Chengdu Cryo-Push Medical Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cold Compression Wrap Pro?
The FDA product code for Cold Compression Wrap Pro is IRP.
Other records listing Chengdu Cryo-Push Medical 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.