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FDA 510(k)

CATHETER, PERITONEAL DIALYSIS

K-Number: K760544 · 1976-10-20

ApplicantTravenol Laboratories, S.A.
Decision Date1976-10-20
Product CodeFKO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, PERITONEAL DIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760544. 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 CATHETER, PERITONEAL DIALYSIS?

CATHETER, PERITONEAL DIALYSIS is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760544.

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

CATHETER, PERITONEAL DIALYSIS received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760544.

Who is the listed applicant for CATHETER, PERITONEAL DIALYSIS?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Other records listing Travenol Laboratories, S.A. 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.

K874181BAXTER BEDSIDE SYSTEMK873894CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITEK873873RESUBMITTED MICRON TRANSFUSION FILTERK873984AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)K872364HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309K872652UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM

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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.K974570PERITONEAL DIALYSIS CATHETER CONNECTORMedigroup, 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.

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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