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FDA 510(k)

ESTECH AORTIC EASY FLOW CANNULA

K-Number: K060101 · 2006-05-10

ApplicantEndoscopic Technologies, Inc.
Decision Date2006-05-10
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESTECH AORTIC EASY FLOW CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 2006-05-10 under 510(k) number K060101. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESTECH AORTIC EASY FLOW CANNULA?

ESTECH AORTIC EASY FLOW CANNULA is a medical device that received FDA 510(k) clearance on 2006-05-10. The listed applicant is Endoscopic Technologies, Inc.. The 510(k) number is K060101.

When did ESTECH AORTIC EASY FLOW CANNULA receive FDA 510(k) clearance?

ESTECH AORTIC EASY FLOW CANNULA received FDA 510(k) clearance on 2006-05-10, under 510(k) number K060101.

Who is the listed applicant for ESTECH AORTIC EASY FLOW CANNULA?

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

What is the FDA product code for ESTECH AORTIC EASY FLOW CANNULA?

The FDA product code for ESTECH AORTIC EASY FLOW CANNULA is DWF.

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Other records listing Endoscopic Technologies, 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.

K053326ESTECH COBRA ELECTROSURGICAL UNIT & CABLEK053100ESTECH COBRA BIPOLAR SYSTEMK946105ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIESK945978TUBING, NONINVASIVEK945979TROCAR/CANNULAK924057DISPOSIBLE ELECTRO COAGULATION PROBE

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Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, 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.

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