Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8

K-Number: K860155 · 1986-02-14

ApplicantMedical Components, Inc.
Decision Date1986-02-14
Product CodeFKO
Advisory CommitteeGU
DecisionUnknown

Device Summary

PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1986-02-14 under 510(k) number K860155. The device is classified under product code FKO. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8?

PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 is a medical device that received FDA 510(k) clearance on 1986-02-14. The listed applicant is Medical Components, Inc.. The 510(k) number is K860155.

When did PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 receive FDA 510(k) clearance?

PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 received FDA 510(k) clearance on 1986-02-14, under 510(k) number K860155.

Who is the listed applicant for PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8?

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

What is the FDA product code for PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8?

The FDA product code for PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Components, 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.

K25083614F Duo-Flow® Side X Side Double Lumen CatheterK1316876F X 60CM TRIPLE PRO-LINE CT BASIC IR SETK1306872F & 3F VASCU-SHEATH TEARAWAY INTRODUCERK1309235F DIGNITY CT TITANIUM PORTK124046VALVED TEARAWAY INTRODUCER GENERATION IIK1236173F PRO-PICC

View all 61 devices →

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.

↑