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FDA 510(k)

CENTRAL VENOUS CATHETER

K-Number: K823351 · 1982-12-09

ApplicantPlasmedics, Inc.
Decision Date1982-12-09
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Plasmedics, Inc.. It received FDA 510(k) clearance on 1982-12-09 under 510(k) number K823351. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VENOUS CATHETER?

CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1982-12-09. The listed applicant is Plasmedics, Inc.. The 510(k) number is K823351.

When did CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1982-12-09, under 510(k) number K823351.

Who is the listed applicant for CENTRAL VENOUS CATHETER?

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

What is the FDA product code for CENTRAL VENOUS CATHETER?

The FDA product code for CENTRAL VENOUS CATHETER is FOZ.

Related Clinical Trials

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.

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Other records listing Plasmedics, 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.

K853559STERILE BIOPSY NEEDLESK850263PEDIATRIC ANESTHESIA MASK W/PACIFIER/RING ASSEMBLYK831601APNEA ALARM FOR ADULT-PEDIATRIC & NEONK831650ANESTHESIA/RESPIRATORY DISCONNECT -K830604WEDGE PRESSURE CATHETER

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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