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FDA 510(k)

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS

K-Number: K894413 · 1989-09-22

ApplicantInmark Corp.
Decision Date1989-09-22
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Inmark Corp.. It received FDA 510(k) clearance on 1989-09-22 under 510(k) number K894413. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1989-09-22. The listed applicant is Inmark Corp.. The 510(k) number is K894413.

When did X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS receive FDA 510(k) clearance?

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS received FDA 510(k) clearance on 1989-09-22, under 510(k) number K894413.

Who is the listed applicant for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

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

What is the FDA product code for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

The FDA product code for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is ITY.

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 Inmark Corp. 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.

K910308X-RAY TUBE HOUSING ASSEMBLY POLARIX II GEN/XO 110K910276X-RAY TUBE HOUSING ASSEMBLY SOREDEX DC/CIR 51K894742RELOADING OF X-RAY TUBE HOUSING ASSEM., VARIOUS

Related Devices (Code: ITY)

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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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