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)

MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

K-Number: K932746 · 1993-07-21

ApplicantTri W-G, Inc.
Decision Date1993-07-21
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE 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 1993-07-21 under 510(k) number K932746. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE?

MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE is a medical device that received FDA 510(k) clearance on 1993-07-21. The listed applicant is Tri W-G, Inc.. The 510(k) number is K932746.

When did MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE receive FDA 510(k) clearance?

MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE received FDA 510(k) clearance on 1993-07-21, under 510(k) number K932746.

Who is the listed applicant for MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE?

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 MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE?

The FDA product code for MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE is INQ.

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 TABLESK930802MODELS 642 & 643 TILT EXAM/TREATMENT TABLE

View all 35 devices →

Related Devices (Code: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

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.

↑