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FDA 510(k)

CHEMO-CATH INTRAPERITONEAL CATHETER

K-Number: K863819 · 1987-02-04

ApplicantHdc Corp.
Decision Date1987-02-04
Product CodeFJS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CHEMO-CATH INTRAPERITONEAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1987-02-04 under 510(k) number K863819. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMO-CATH INTRAPERITONEAL CATHETER?

CHEMO-CATH INTRAPERITONEAL CATHETER is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Hdc Corp.. The 510(k) number is K863819.

When did CHEMO-CATH INTRAPERITONEAL CATHETER receive FDA 510(k) clearance?

CHEMO-CATH INTRAPERITONEAL CATHETER received FDA 510(k) clearance on 1987-02-04, under 510(k) number K863819.

Who is the listed applicant for CHEMO-CATH INTRAPERITONEAL CATHETER?

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

What is the FDA product code for CHEMO-CATH INTRAPERITONEAL CATHETER?

The FDA product code for CHEMO-CATH INTRAPERITONEAL CATHETER is FJS.

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Other records listing Hdc Corp. 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.

K071875V-CATH POLY PICCK023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BGK033853MODIFICATION TO V-CATH POLY PICCK032404SELDINGER SAFETY NEEDLE INTRODUCERK022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S

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Related Devices (Code: FJS)

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.

K213602Argyle Peritoneal Dialysis Cathetor and Kit, Ritus Peritoneal Dialysis Catheter Tunneling Tool KitCovidien, LLCK180485Argyle Peritoneal Dialysis Catheter and Kits, Argyle Presternal Peritoneal Dialysis Catheter and Kits, Argyle Peritoneal Dialysis Accessory Two Part Titanium Luer Adapter, Argyle Adult Peritoneal Dialysis Accessory Titanium Catheter ExtenderCovidien, LLCK130441FALLER STYLETMedionics International, Inc.K121383PS X SERIES (BASIC COMPONENTS AND CATHETER), PD X SERIES (CATHETER WITH ALL COMPONENTS)Medical Components, Inc.K120130FALLER TROCARMedigroup, Inc.K113354VETA PERITONEAL DIALYSIS CATHETERPfm Medical, 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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