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FDA 510(k)

TROCAR CATHETER/THORACIC CATHETER

K-Number: K792202 · 1979-11-20

ApplicantPortex, Inc.
Decision Date1979-11-20
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TROCAR CATHETER/THORACIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Portex, Inc.. It received FDA 510(k) clearance on 1979-11-20 under 510(k) number K792202. 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 TROCAR CATHETER/THORACIC CATHETER?

TROCAR CATHETER/THORACIC CATHETER is a medical device that received FDA 510(k) clearance on 1979-11-20. The listed applicant is Portex, Inc.. The 510(k) number is K792202.

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

TROCAR CATHETER/THORACIC CATHETER received FDA 510(k) clearance on 1979-11-20, under 510(k) number K792202.

Who is the listed applicant for TROCAR CATHETER/THORACIC CATHETER?

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

What is the FDA product code for TROCAR CATHETER/THORACIC CATHETER?

The FDA product code for TROCAR CATHETER/THORACIC CATHETER is DWF.

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Other records listing Portex, 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.

K033080PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETERK031057PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KITK0237931ST RESPONSE INTERMEDIATE MANUAL RESUSCITATORK0141151ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XXK014073HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICEK873992LARYNGECTOMY TUBE

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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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