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FDA 510(k)

CHASE THORACIC CATHETER

K-Number: K971023 · 1997-09-08

ApplicantChase Medical, Inc.
Decision Date1997-09-08
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHASE THORACIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Chase Medical, Inc.. It received FDA 510(k) clearance on 1997-09-08 under 510(k) number K971023. 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 CHASE THORACIC CATHETER?

CHASE THORACIC CATHETER is a medical device that received FDA 510(k) clearance on 1997-09-08. The listed applicant is Chase Medical, Inc.. The 510(k) number is K971023.

When did CHASE THORACIC CATHETER receive FDA 510(k) clearance?

CHASE THORACIC CATHETER received FDA 510(k) clearance on 1997-09-08, under 510(k) number K971023.

Who is the listed applicant for CHASE THORACIC CATHETER?

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

What is the FDA product code for CHASE THORACIC CATHETER?

The FDA product code for CHASE THORACIC CATHETER is DWF.

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Other records listing Chase Medical, 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.

K032531CHASE CARDIAC ANALYSIS SYSTEMK022093CHASE CARDIOVASCULAR PATCH KITK021129CHARE CARIOVASCULAR PATCHK020233CHASE CARDIOVASCULAR PATCH KITK020132CHASE CARDIOVASCULAR PATCH KITK012248CHASE CARDIOVASCULAR PATCH

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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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