Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

JetBoots PRO Plus

K-Number: K241256 · 2024-08-30

ApplicantTherabody, Inc.
Decision Date2024-08-30
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JetBoots PRO Plus is a medical device manufactured by Therabody, Inc.. It received FDA 510(k) clearance on 2024-08-30 under approval number K241256. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Therabody, Inc.. The 510(k) number is K241256.

When was JetBoots PRO Plus approved by the FDA?

JetBoots PRO Plus received FDA 510(k) clearance on 2024-08-30, under approval number K241256.

What company makes JetBoots PRO Plus?

JetBoots PRO Plus is manufactured by Therabody, Inc..

What is the FDA product code for JetBoots PRO Plus?

The FDA product code for JetBoots PRO Plus is IRP.

Other Devices by Therabody, Inc.

K230293TheraFace Mask

Related Devices (Code: IRP)

K160608NormaTec Pulse and NormaTec Pulse ProNormaTec Industries, LP K171685Med4 EliteCool Systems, Inc. (Dba Game Ready) K161907Pressure Therapy SystemXiamen Senyang Co., Ltd. K163280RP Lite 760RMego Afek AC , Ltd. K160178Lympha-Flow(LF1200)Daesung Maref Co., Ltd. K183169Pulse 2.0, Pulse Pro 2.0NormaTec Industries, LP

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.

↑