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FDA 510(k)

PERITONEAL DIALYSIS CATHETER CONNECTOR

K-Number: K974570 · 1998-02-27

ApplicantMedigroup, Inc.
Decision Date1998-02-27
Product CodeFKO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS CATHETER CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medigroup, Inc.. It received FDA 510(k) clearance on 1998-02-27 under 510(k) number K974570. The device is classified under product code FKO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITONEAL DIALYSIS CATHETER CONNECTOR?

PERITONEAL DIALYSIS CATHETER CONNECTOR is a medical device that received FDA 510(k) clearance on 1998-02-27. The listed applicant is Medigroup, Inc.. The 510(k) number is K974570.

When did PERITONEAL DIALYSIS CATHETER CONNECTOR receive FDA 510(k) clearance?

PERITONEAL DIALYSIS CATHETER CONNECTOR received FDA 510(k) clearance on 1998-02-27, under 510(k) number K974570.

Who is the listed applicant for PERITONEAL DIALYSIS CATHETER CONNECTOR?

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

What is the FDA product code for PERITONEAL DIALYSIS CATHETER CONNECTOR?

The FDA product code for PERITONEAL DIALYSIS CATHETER CONNECTOR is FKO.

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 Medigroup, 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.

K120130FALLER TROCARK071167FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560K070730FLEX-NECK ARC CATHETERK060897EMBEDDING TOOL, MODEL TE-1000K031351FLEX-NECK PD CATHETER, INFANT

Related Devices (Code: FKO)

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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISCorpak, Inc.K910787TITANIUM CONNECTOR (2 PART)Accurate Surgical Instruments Co.K885037AMUKIN 50% - AIRSPRAY(R)Bernard J. Cooney, P.A.K874650PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)Quinton, Inc.K872221DIALY-NATE SET & DIALY-NATE CATHETERGesco Intl., Inc.K871730MODIFIED USE OF PULL-APART INTRODUCER SETQuinton, 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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