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FDA 510(k)

CANNULA, HUNTER-SESSIONS, SELF-RETAIN.

K-Number: K770068 · 1977-03-01

ApplicantBarlow Mfg., Corp.
Decision Date1977-03-01
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CANNULA, HUNTER-SESSIONS, SELF-RETAIN. is the device name listed in this FDA 510(k) record. The listed applicant is Barlow Mfg., Corp.. It received FDA 510(k) clearance on 1977-03-01 under 510(k) number K770068. 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 CANNULA, HUNTER-SESSIONS, SELF-RETAIN.?

CANNULA, HUNTER-SESSIONS, SELF-RETAIN. is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Barlow Mfg., Corp.. The 510(k) number is K770068.

When did CANNULA, HUNTER-SESSIONS, SELF-RETAIN. receive FDA 510(k) clearance?

CANNULA, HUNTER-SESSIONS, SELF-RETAIN. received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770068.

Who is the listed applicant for CANNULA, HUNTER-SESSIONS, SELF-RETAIN.?

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

What is the FDA product code for CANNULA, HUNTER-SESSIONS, SELF-RETAIN.?

The FDA product code for CANNULA, HUNTER-SESSIONS, SELF-RETAIN. 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

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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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