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FDA 510(k)

LIFEMED LIFECOIL CATHETERS

K-Number: K841929 · 1984-08-08

ApplicantLifemed of California
Decision Date1984-08-08
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIFEMED LIFECOIL CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Lifemed of California. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K841929. 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 LIFEMED LIFECOIL CATHETERS?

LIFEMED LIFECOIL CATHETERS is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Lifemed of California. The 510(k) number is K841929.

When did LIFEMED LIFECOIL CATHETERS receive FDA 510(k) clearance?

LIFEMED LIFECOIL CATHETERS received FDA 510(k) clearance on 1984-08-08, under 510(k) number K841929.

Who is the listed applicant for LIFEMED LIFECOIL CATHETERS?

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

What is the FDA product code for LIFEMED LIFECOIL CATHETERS?

The FDA product code for LIFEMED LIFECOIL CATHETERS is FKX.

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 Lifemed of California 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.

K001329INTRAVASCULAR IV SET, IV SET WITH BURETTE, EXTENSION SETK903502LIFECOIL CATHETERK821624LOW VOLUME INFUSTION SET

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

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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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