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)

REBAR MICRO CATHETER, MODELS 105-5080, 105-5086

K-Number: K993672 · 2000-01-04

ApplicantMicro Therapeutics, Inc.
Decision Date2000-01-04
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REBAR MICRO CATHETER, MODELS 105-5080, 105-5086 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc.. It received FDA 510(k) clearance on 2000-01-04 under 510(k) number K993672. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REBAR MICRO CATHETER, MODELS 105-5080, 105-5086?

REBAR MICRO CATHETER, MODELS 105-5080, 105-5086 is a medical device that received FDA 510(k) clearance on 2000-01-04. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K993672.

When did REBAR MICRO CATHETER, MODELS 105-5080, 105-5086 receive FDA 510(k) clearance?

REBAR MICRO CATHETER, MODELS 105-5080, 105-5086 received FDA 510(k) clearance on 2000-01-04, under 510(k) number K993672.

Who is the listed applicant for REBAR MICRO CATHETER, MODELS 105-5080, 105-5086?

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

What is the FDA product code for REBAR MICRO CATHETER, MODELS 105-5080, 105-5086?

The FDA product code for REBAR MICRO CATHETER, MODELS 105-5080, 105-5086 is KRA.

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 Micro Therapeutics, 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.

K113289ORION MICRO CATHETERK11345414 WIRE STANDARD, 14 WIRE LSK090870ECHELON MICRO CATHETER, MODELS 105-5092-150SA, 145-5092-150SA AND 190-5092-150SA AND SYRINGE ADAPTER ACCESSORYK090046CONCERTO DETACHABLE COIL SYSTEMK081465AXIUM DETACHABLE COIL SYSTEMK060747FX DETACHABLE COIL SYSTEM

View all 51 devices →

Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

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.

↑