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)

UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES

K-Number: K070331 · 2007-05-04

ApplicantLaborie Medical Technologies
Decision Date2007-05-04
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Laborie Medical Technologies. It received FDA 510(k) clearance on 2007-05-04 under 510(k) number K070331. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES?

UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2007-05-04. The listed applicant is Laborie Medical Technologies. The 510(k) number is K070331.

When did UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES receive FDA 510(k) clearance?

UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES received FDA 510(k) clearance on 2007-05-04, under 510(k) number K070331.

Who is the listed applicant for UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES?

The FDA 510(k) record lists Laborie Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES?

The FDA product code for UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES is KPI.

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

Related Devices (Code: KPI)

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.

K262353BTL-299-FBTL Industries, Inc.K260178Pelvic Muscle Trainer (KM510, KM516B)Shenzhen Konmed Technology Co., Ltd.K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer (PC22E); Pelvic Muscle Trainer (PC22E-L)Hunan Accurate Bio-Medical Technology Co., Ltd.K252552Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)Shenzhen Changkun Technology Co., Ltd.K252831Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)Dolanvy (Suzhou) Medical Technology Co., Ltd.K252334PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)Pontemedag

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.

↑