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FDA 510(k)

RIGHT ATRIAL CATHETER INSERTION TRAY

K-Number: K881352 · 1988-06-09

ApplicantQuinton, Inc.
Decision Date1988-06-09
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RIGHT ATRIAL CATHETER INSERTION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1988-06-09 under 510(k) number K881352. 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 RIGHT ATRIAL CATHETER INSERTION TRAY?

RIGHT ATRIAL CATHETER INSERTION TRAY is a medical device that received FDA 510(k) clearance on 1988-06-09. The listed applicant is Quinton, Inc.. The 510(k) number is K881352.

When did RIGHT ATRIAL CATHETER INSERTION TRAY receive FDA 510(k) clearance?

RIGHT ATRIAL CATHETER INSERTION TRAY received FDA 510(k) clearance on 1988-06-09, under 510(k) number K881352.

Who is the listed applicant for RIGHT ATRIAL CATHETER INSERTION TRAY?

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

What is the FDA product code for RIGHT ATRIAL CATHETER INSERTION TRAY?

The FDA product code for RIGHT ATRIAL CATHETER INSERTION TRAY is DWF.

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Other records listing Quinton, 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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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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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