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FDA 510(k)

CRISA

K-Number: K833847 · 1983-12-12

ApplicantX-Ray Tube Corp.
Decision Date1983-12-12
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CRISA is the device name listed in this FDA 510(k) record. The listed applicant is X-Ray Tube Corp.. It received FDA 510(k) clearance on 1983-12-12 under 510(k) number K833847. 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 CRISA?

CRISA is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is X-Ray Tube Corp.. The 510(k) number is K833847.

When did CRISA receive FDA 510(k) clearance?

CRISA received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833847.

Who is the listed applicant for CRISA?

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

What is the FDA product code for CRISA?

The FDA product code for CRISA 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 X-Ray Tube 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.

K840135CRISAK833238CRISA

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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