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)

XMA INTEGRATED TABLE

K-Number: K850118 · 1985-04-09

ApplicantSummit Industries, Inc.
Decision Date1985-04-09
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XMA INTEGRATED TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Summit Industries, Inc.. It received FDA 510(k) clearance on 1985-04-09 under 510(k) number K850118. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XMA INTEGRATED TABLE?

XMA INTEGRATED TABLE is a medical device that received FDA 510(k) clearance on 1985-04-09. The listed applicant is Summit Industries, Inc.. The 510(k) number is K850118.

When did XMA INTEGRATED TABLE receive FDA 510(k) clearance?

XMA INTEGRATED TABLE received FDA 510(k) clearance on 1985-04-09, under 510(k) number K850118.

Who is the listed applicant for XMA INTEGRATED TABLE?

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

What is the FDA product code for XMA INTEGRATED TABLE?

The FDA product code for XMA INTEGRATED TABLE is IXQ.

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 Summit Industries, 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.

K874908C900 X-RAY FILM PROCESSORK874687COLLI-MATETM MODEL NO. B800K851440RDIOGRAPHIC WALL HOLDER OR FILM RECEPTORK850198FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOGK850117XMA 325 (X-RAY GENERATOR)

Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, 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.

↑