JetBoots PRO Plus
K-Number: K241256 · 2024-08-30
Device Summary
Frequently Asked Questions
What is the JetBoots PRO Plus?
JetBoots PRO Plus is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Therabody, Inc.. The 510(k) number is K241256.
When did JetBoots PRO Plus receive FDA 510(k) clearance?
JetBoots PRO Plus received FDA 510(k) clearance on 2024-08-30, under 510(k) number K241256.
Who is the listed applicant for JetBoots PRO Plus?
The FDA 510(k) record lists Therabody, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JetBoots PRO Plus?
The FDA product code for JetBoots PRO Plus is IRP.
Other records listing Therabody, Inc. 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.