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FDA 510(k)

STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP

K-Number: K994209 · 2000-06-14

ApplicantCobe Cardiovascular, Inc.
Decision Date2000-06-14
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Cardiovascular, Inc.. It received FDA 510(k) clearance on 2000-06-14 under 510(k) number K994209. 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 STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP?

STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP is a medical device that received FDA 510(k) clearance on 2000-06-14. The listed applicant is Cobe Cardiovascular, Inc.. The 510(k) number is K994209.

When did STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP receive FDA 510(k) clearance?

STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP received FDA 510(k) clearance on 2000-06-14, under 510(k) number K994209.

Who is the listed applicant for STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP?

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

What is the FDA product code for STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP?

The FDA product code for STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP is DWF.

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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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