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)

FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB

K-Number: K904722 · 1991-01-23

ApplicantTri W-G, Inc.
Decision Date1991-01-23
Product Code
DecisionSubstantially Equivalent

Device Summary

FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB 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 1991-01-23 under 510(k) number K904722. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB?

FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB is a medical device that received FDA 510(k) clearance on 1991-01-23. The listed applicant is Tri W-G, Inc.. The 510(k) number is K904722.

When did FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB receive FDA 510(k) clearance?

FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB received FDA 510(k) clearance on 1991-01-23, under 510(k) number K904722.

Who is the listed applicant for FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB?

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

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 →

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.

↑