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FDA 510(k)

AUTOMATIC PERITONEAL DIALYSIS CYCLER

K-Number: K833065 · 1983-11-28

ApplicantTravenol Laboratories, S.A.
Decision Date1983-11-28
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC PERITONEAL DIALYSIS CYCLER 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 1983-11-28 under 510(k) number K833065. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC PERITONEAL DIALYSIS CYCLER?

AUTOMATIC PERITONEAL DIALYSIS CYCLER is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K833065.

When did AUTOMATIC PERITONEAL DIALYSIS CYCLER receive FDA 510(k) clearance?

AUTOMATIC PERITONEAL DIALYSIS CYCLER received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833065.

Who is the listed applicant for AUTOMATIC PERITONEAL DIALYSIS CYCLER?

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 AUTOMATIC PERITONEAL DIALYSIS CYCLER?

The FDA product code for AUTOMATIC PERITONEAL DIALYSIS CYCLER is FKX.

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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

View all 206 devices →

Related Devices (Code: FKX)

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.

K250523Archimedes Pro Automated Peritoneal Dialysis Cycler (3014-00000-1); Archimedes Standard Automated Peritoneal Dialysis Cycler (3014-00000-3); Archimedes Pro Disposable Tubing Set (3014-50000-1); Archimedes Standard Disposable Tubing Set (3014-50000-3); Archimedes Pro Plus Disposable Tubing Set (3014-50000-5)Simergent, LLCK243371Byonyks X-1 APD Cycler; Byonyks Automated PD Set DS-1Byonyks Pvt, Ltd.K220935Digital Dialysis Clinic - Intelligent Dialysis Assistant (IDA) with Medical Supervision Portal and IDA Smartphone AppIren-Medical, Ltd.K222318Fresenius Liberty Select CyclerFresenius Medical Care Renal Therapies Group, LLCK212522Lilliput APD SystemFresenius Medical Care Renal Therapies Group, LLCK212658CloudCath Peritoneal Dialysis Drain Set Monitoring SystemCloudcath

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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