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)

KENDALL-LTP TURNER SAVE-A-LINE

K-Number: K003511 · 2001-01-24

ApplicantThe Ludlow Company LP
Decision Date2001-01-24
Product CodeFRP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KENDALL-LTP TURNER SAVE-A-LINE is the device name listed in this FDA 510(k) record. The listed applicant is The Ludlow Company LP. It received FDA 510(k) clearance on 2001-01-24 under 510(k) number K003511. The device is classified under product code FRP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDALL-LTP TURNER SAVE-A-LINE?

KENDALL-LTP TURNER SAVE-A-LINE is a medical device that received FDA 510(k) clearance on 2001-01-24. The listed applicant is The Ludlow Company LP. The 510(k) number is K003511.

When did KENDALL-LTP TURNER SAVE-A-LINE receive FDA 510(k) clearance?

KENDALL-LTP TURNER SAVE-A-LINE received FDA 510(k) clearance on 2001-01-24, under 510(k) number K003511.

Who is the listed applicant for KENDALL-LTP TURNER SAVE-A-LINE?

The FDA 510(k) record lists The Ludlow Company LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL-LTP TURNER SAVE-A-LINE?

The FDA product code for KENDALL-LTP TURNER SAVE-A-LINE is FRP.

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 The Ludlow Company LP 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.

K021132UNI-PATCH ULTRASOUND COUPLING GELK012218LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES

Related Devices (Code: FRP)

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.

K082367INFANT SLEEP BEANIELife Innovations, LLCK090284RES-Q INFANT WEDGE AND SLINGCr Enterprises, LLCK062143KOZY COMFORT INFANT POSITIONERAlfred E Mann Inst. For Biomedical EngineeringK060986HEAD BEDSteven H. Warnock, M.D.K051300ROBIN HOOD VESTKamber CorporationK041996NIGHTFORMPlastic Surgery Solutions, LLC

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.

↑