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

FDA 510(k)

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM

K-Number: K030876 · 2004-01-22

ApplicantCynosure, Inc.
Decision Date2004-01-22
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cynosure, Inc.. It received FDA 510(k) clearance on 2004-01-22 under 510(k) number K030876. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM?

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-22. The listed applicant is Cynosure, Inc.. The 510(k) number is K030876.

When did CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM receive FDA 510(k) clearance?

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM received FDA 510(k) clearance on 2004-01-22, under 510(k) number K030876.

Who is the listed applicant for CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM?

The FDA 510(k) record lists Cynosure, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM?

The FDA product code for CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM is ISA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cynosure, 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.

K190678TempSureK182365TempSure SystemK173199PicoSure WorkstationK171992SculpSureK171262TempSureK171111Sculpsure

View all 88 devices →

Related Devices (Code: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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.

↑