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)

ADULT WALKING HEEL PRODUCT NO. 4183-130

K-Number: K873716 · 1987-10-02

ApplicantMartin Medical
Decision Date1987-10-02
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADULT WALKING HEEL PRODUCT NO. 4183-130 is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1987-10-02 under 510(k) number K873716. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT WALKING HEEL PRODUCT NO. 4183-130?

ADULT WALKING HEEL PRODUCT NO. 4183-130 is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Martin Medical. The 510(k) number is K873716.

When did ADULT WALKING HEEL PRODUCT NO. 4183-130 receive FDA 510(k) clearance?

ADULT WALKING HEEL PRODUCT NO. 4183-130 received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873716.

Who is the listed applicant for ADULT WALKING HEEL PRODUCT NO. 4183-130?

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

What is the FDA product code for ADULT WALKING HEEL PRODUCT NO. 4183-130?

The FDA product code for ADULT WALKING HEEL PRODUCT NO. 4183-130 is LDF.

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 Martin Medical 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.

K873723PLASTER VACUUM, 230V MODEL NO. 4183-161K873721PLASTER VACUUM, 115V MODEL NO. 4183-160K873719CAST CUTTER, 115V MODEL NO. 4183-106K873722PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873720CAST CUTTER, 230V MODEL NO. 4183-107K873717CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135

View all 14 devices →

Related Devices (Code: LDF)

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.

K252042Sync AV II Temporary Pacing CatheterSwift Sync, Inc.K242863Bioptimal Bipolar Pacing CatheterBioptimal International Pte. , Ltd.K251186Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer)C.R. Bard, Inc.K241334Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 4Fr. (006221P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 5Fr. (006225P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 6Fr. (006241P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 7Fr. (006242P); NBIH™ Temporary Pacing Electrode Catheter,C.R. Bard, Inc.K241199Rotatable Connector (5944RL)Shenzhen Launch Electrical Co., Ltd.K242705Streamline Unipolar Pediatric Temporary Pacing Lead (6491) Streamline Unipolar Temporary Atrial Pacing Lead (6492) Streamline Unipolar Temporary Myocardial Pacing Wire (6494) Streamline Bipolar Temporary Myocardial Pacing Lead (6495) Streamline Unipolar Temporary Myocardial Pacing Lead (6500)Medtronic, 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.

↑