FDA 510(k) Application Details - K242140

Device Classification Name Massager, Powered Inflatable Tube

  More FDA Info for this Device
510(K) Number K242140
Device Name Massager, Powered Inflatable Tube
Applicant Jiale Health Technology Shenzhen Co., Ltd.
201, Builing A, No, 17, Guangjin Road, Shapu Community,
Songgang Street, Bao 'an District
Shenzhen 518000 CN
Other 510(k) Applications for this Company
Contact Lixun Xie
Other 510(k) Applications for this Contact
Regulation Number 890.5650

  More FDA Info for this Regulation Number
Classification Product Code IRP
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 07/22/2024
Decision Date 03/17/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee PM - Physical Medicine
Review Advisory Committee PM - Physical Medicine
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K242140


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact