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)

TUBE, LEAD, AND CORD HOLDER NO. 102

K-Number: K924568 · 1992-11-23

ApplicantAnsley Medical Products, Inc.
Decision Date1992-11-23
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBE, LEAD, AND CORD HOLDER NO. 102 is the device name listed in this FDA 510(k) record. The listed applicant is Ansley Medical Products, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K924568. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE, LEAD, AND CORD HOLDER NO. 102?

TUBE, LEAD, AND CORD HOLDER NO. 102 is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Ansley Medical Products, Inc.. The 510(k) number is K924568.

When did TUBE, LEAD, AND CORD HOLDER NO. 102 receive FDA 510(k) clearance?

TUBE, LEAD, AND CORD HOLDER NO. 102 received FDA 510(k) clearance on 1992-11-23, under 510(k) number K924568.

Who is the listed applicant for TUBE, LEAD, AND CORD HOLDER NO. 102?

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

What is the FDA product code for TUBE, LEAD, AND CORD HOLDER NO. 102?

The FDA product code for TUBE, LEAD, AND CORD HOLDER NO. 102 is KMK.

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 Ansley Medical Products, 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.

K932857ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.K925290CATALOG NUMBER 111 (FACESHIELD)K924567FOLEY CATHETER TUBE HOLDER NO. 101K924566RESTRAINT, PROTECTIVE N0. 103

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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.

↑