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)

MOTORIZED PARALLEL BAR, MODEL 110

K-Number: K882916 · 1988-07-28

ApplicantTri W-G, Inc.
Decision Date1988-07-28
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOTORIZED PARALLEL BAR, MODEL 110 is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882916. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTORIZED PARALLEL BAR, MODEL 110?

MOTORIZED PARALLEL BAR, MODEL 110 is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Tri W-G, Inc.. The 510(k) number is K882916.

When did MOTORIZED PARALLEL BAR, MODEL 110 receive FDA 510(k) clearance?

MOTORIZED PARALLEL BAR, MODEL 110 received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882916.

Who is the listed applicant for MOTORIZED PARALLEL BAR, MODEL 110?

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

What is the FDA product code for MOTORIZED PARALLEL BAR, MODEL 110?

The FDA product code for MOTORIZED PARALLEL BAR, MODEL 110 is BXB.

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 Tri W-G, 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.

K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777K945163ECHOCARDIOGRAPHYK941720MODEL 747 AND 747-30 EXAM/TREATMENT TABLEK936303TREATMENT TABLE MODIFICATIONK933119HI-LO TREATMENT TABLESK932746MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

View all 35 devices →

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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.

↑