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FDA 510(k)

CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS

K-Number: K893499 · 1989-11-16

ApplicantCmsi
Decision Date1989-11-16
Product CodeEQJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS is the device name listed in this FDA 510(k) record. The listed applicant is Cmsi. It received FDA 510(k) clearance on 1989-11-16 under 510(k) number K893499. The device is classified under product code EQJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS?

CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS is a medical device that received FDA 510(k) clearance on 1989-11-16. The listed applicant is Cmsi. The 510(k) number is K893499.

When did CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS receive FDA 510(k) clearance?

CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS received FDA 510(k) clearance on 1989-11-16, under 510(k) number K893499.

Who is the listed applicant for CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS?

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

What is the FDA product code for CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS?

The FDA product code for CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS is EQJ.

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 Cmsi 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.

K790169TOMOGRAPHIC PROGRAMSK790168COLLIMATOR, BILATERIAL

Related Devices (Code: EQJ)

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.

K161514Precision Thin Reciprocating Blade, 0.010in.Stryker CorporationK041985XPS CURVED BURMedtronic Xomed, Inc.K974232ESSENTIAL SHAVER SYSTEMGyrus Ent LLCK960853ACE SYSTEMXomed, Inc.K955704TREBAY MICRODEBRIDER SYSTEMTrebay Medical Corp.K955294SOF - ABRASION BURTrebay Medical 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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